Canonical Allele Identifier: CA849634475

Gene:

Linked Data

• dbSNP Id: rs1241188163
• MyVariant Identifiers: chr8:g.19987673G>A (hg19) ; chr8:g.20130162G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20130162G>A , CM000670.2:g.20130162G>A	GRCh38
NC_000008.10:g.19987673G>A , CM000670.1:g.19987673G>A	GRCh37
NC_000008.9:g.20031953G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949563.1:n.3408+243G>A
XR_949563.2:n.3400+243G>A