Canonical Allele Identifier: CA832742489
Gene:

Linked Data

dbSNP Id: rs956236610

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306320A>T , CM000669.2:g.124306320A>T GRCh38
NC_000007.13:g.123946374A>T , CM000669.1:g.123946374A>T GRCh37
NC_000007.12:g.123733610A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-158A>T