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Select item 32105311.

rs3210531 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:46428800 (GRCh38)
11:46450350 (GRCh37)
Canonical SPDI:: NC_000011.10:46428799:G:A,NC_000011.10:46428799:G:C
Gene:: AMBRA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000011.10:g.46428800G>A, NC_000011.10:g.46428800G>C, NC_000011.9:g.46450350G>A, NC_000011.9:g.46450350G>C, NG_011275.5:g.682C>T, NG_011275.5:g.682C>G

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3210531[uid] (1)
SNP
69370884[uid] (0)
SNP
4646149[uid] (1)
SNP
Bos taurus chromosome 1 genomic contig, reference assembly (based on Btau_3.1), ...
Bos taurus chromosome 1 genomic contig, reference assembly (based on Btau_3.1), whole genome shotgun sequence
gi|119879628|ref|NW_001493888.1|Bt1 8_3

Nucleotide
Bos taurus integrin subunit beta 5 (ITGB5), mRNA
Bos taurus integrin subunit beta 5 (ITGB5), mRNA
gi|31340754|ref|NM_174679.2|

Nucleotide

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