Canonical Allele Identifier: CA821223493
Gene:

Linked Data

dbSNP Id: rs1313226564

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812357T>C , CM000668.2:g.155812357T>C GRCh38
NC_000006.11:g.156133491T>C , CM000668.1:g.156133491T>C GRCh37
NC_000006.10:g.156175183T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18938T>C
XR_943146.1:n.645-318A>G
XR_001744423.1:n.699-318A>G
XR_001744424.1:n.79+18938T>C