Canonical Allele Identifier: CA185510876

Gene:

Linked Data

• dbSNP Id: rs921934936
• MyVariant Identifiers: chr8:g.126490659T>C (hg19) ; chr8:g.125478417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478417T>C , CM000670.2:g.125478417T>C	GRCh38
NC_000008.10:g.126490659T>C , CM000670.1:g.126490659T>C	GRCh37
NC_000008.9:g.126559841T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5103T>C