Canonical Allele Identifier: CA1740470112
Gene:

Linked Data

dbSNP Id: rs1795646176

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306341A>T , CM000669.2:g.124306341A>T GRCh38
NC_000007.13:g.123946395A>T , CM000669.1:g.123946395A>T GRCh37
NC_000007.12:g.123733631A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-137A>T