Canonical Allele Identifier: CA846959086

Gene:

Linked Data

• dbSNP Id: rs1214689166
• MyVariant Identifiers: chr8:g.126490745C>A (hg19) ; chr8:g.125478503C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478503C>A , CM000670.2:g.125478503C>A	GRCh38
NC_000008.10:g.126490745C>A , CM000670.1:g.126490745C>A	GRCh37
NC_000008.9:g.126559927C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5189C>A