Canonical Allele Identifier: CA1689218194
Gene:

Linked Data

dbSNP Id: rs1783119063

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400636C>T , CM000669.2:g.13400636C>T GRCh38
NC_000007.13:g.13440261C>T , CM000669.1:g.13440261C>T GRCh37
NC_000007.12:g.13406786C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90313C>T