Canonical Allele Identifier: CA857362155

Gene:

Linked Data

• dbSNP Id: rs1198789431
• MyVariant Identifiers: chr8:g.98281818G>A (hg19) ; chr8:g.97269590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269590G>A , CM000670.2:g.97269590G>A	GRCh38
NC_000008.10:g.98281818G>A , CM000670.1:g.98281818G>A	GRCh37
NC_000008.9:g.98350994G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149480C>T