Canonical Allele Identifier: CA185510873

Gene:

Linked Data

• dbSNP Id: rs1024905404
• MyVariant Identifiers: chr8:g.126490630G>A (hg19) ; chr8:g.125478388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478388G>A , CM000670.2:g.125478388G>A	GRCh38
NC_000008.10:g.126490630G>A , CM000670.1:g.126490630G>A	GRCh37
NC_000008.9:g.126559812G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5074G>A