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Select item 48979091.

rs4897909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:121742906 (GRCh38)
1:121484704 (GRCh37)
Canonical SPDI:: NC_000001.11:121742905:A:G,NC_000001.11:121742905:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD_genomes)
HGVS:: NC_000001.11:g.121742906A>G, NC_000001.11:g.121742906A>T, NC_000001.10:g.121484704A>G, NC_000001.10:g.121484704A>T, NG_092017.1:g.678A>G, NG_092017.1:g.678A>T, NG_098414.1:g.23A>G, NG_098414.1:g.23A>T

4897909[uid] (1)
SNP
28944221[uid] (1)
SNP
28944222[uid] (1)
SNP
Homo sapiens DNA ligase 1 (LIG1), transcript variant 1, mRNA
Homo sapiens DNA ligase 1 (LIG1), transcript variant 1, mRNA
gi|1519312512|ref|NM_000234.3|

Nucleotide
11879148[uid] (1)
SNP

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