Canonical Allele Identifier: CA1740470137
Gene:

Linked Data

dbSNP Id: rs1395958122

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306385A>T , CM000669.2:g.124306385A>T GRCh38
NC_000007.13:g.123946439A>T , CM000669.1:g.123946439A>T GRCh37
NC_000007.12:g.123733675A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-93A>T