Canonical Allele Identifier: CA2715793882
Gene:

Linked Data

dbSNP Id: rs2116479988

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306258T>C , CM000669.2:g.124306258T>C GRCh38
NC_000007.13:g.123946312T>C , CM000669.1:g.123946312T>C GRCh37
NC_000007.12:g.123733548T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-220T>C