Canonical Allele Identifier: CA1462694334
Gene:

Linked Data

dbSNP Id: rs961093849

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558346A>G , CM000666.2:g.62558346A>G GRCh38
NC_000004.11:g.63424064A>G , CM000666.1:g.63424064A>G GRCh37
NC_000004.10:g.63106659A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5498A>G