Canonical Allele Identifier: CA846959102

Gene:

Linked Data

• dbSNP Id: rs1232721235
• MyVariant Identifiers: chr8:g.126490754T>C (hg19) ; chr8:g.125478512T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478512T>C , CM000670.2:g.125478512T>C	GRCh38
NC_000008.10:g.126490754T>C , CM000670.1:g.126490754T>C	GRCh37
NC_000008.9:g.126559936T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5198T>C