Canonical Allele Identifier: CA1740470114
Gene:

Linked Data

dbSNP Id: rs116895242

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306349T>C , CM000669.2:g.124306349T>C GRCh38
NC_000007.13:g.123946403T>C , CM000669.1:g.123946403T>C GRCh37
NC_000007.12:g.123733639T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-129T>C