Canonical Allele Identifier: CA185510869

Gene:

Linked Data

• dbSNP Id: rs575820826
• MyVariant Identifiers: chr8:g.126490576C>A (hg19) ; chr8:g.125478334C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478334C>A , CM000670.2:g.125478334C>A	GRCh38
NC_000008.10:g.126490576C>A , CM000670.1:g.126490576C>A	GRCh37
NC_000008.9:g.126559758C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5020C>A