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Select item 289288801.

rs28928880 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:176790 (GRCh38)
16:226789 (GRCh37)
Canonical SPDI:: NC_000016.10:176789:A:G
Gene:: HBA1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Clinical significance:: other
Validated:: by cluster
HGVS:: NC_000016.10:g.176790A>G, NC_000016.9:g.226789A>G, NG_000006.1:g.37653A>G, NG_059186.1:g.5140A>G, NM_000558.5:c.74A>G, NM_000558.4:c.74A>G, NM_000558.3:c.74A>G, NG_046166.1:g.2273A>G, NP_000549.1:p.Tyr25Cys

Supplemental Content

28928880[uid] (1)
SNP
503351[uid] (1)
SNP
Homo sapiens chromosome 11 genomic contig, reference assembly
Homo sapiens chromosome 11 genomic contig, reference assembly
gi|51468697|ref|NT_033899.7|Hs11_34

Nucleotide
Homo sapiens interleukin 18 (interferon-gamma-inducing factor) (IL18), mRNA
Homo sapiens interleukin 18 (interferon-gamma-inducing factor) (IL18), mRNA
gi|27502389|ref|NM_001562.2|

Nucleotide
300[uid] (1)
SNP

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