Canonical Allele Identifier: CA1740470153

Gene:

Linked Data

• dbSNP Id: rs1795646904

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306416T>C , CM000669.2:g.124306416T>C	GRCh38
NC_000007.13:g.123946470T>C , CM000669.1:g.123946470T>C	GRCh37
NC_000007.12:g.123733706T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002956584.1:n.73-62T>C