Canonical Allele Identifier: CA580513178

Gene:

Linked Data

• dbSNP Id: rs1199756306
• gnomAD v2: 8-19987763-G-A
• gnomAD v3: 8-20130252-G-A
• gnomAD v4: 8-20130252-G-A
• MyVariant Identifiers: chr8:g.19987763G>A (hg19) ; chr8:g.20130252G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20130252G>A , CM000670.2:g.20130252G>A	GRCh38
NC_000008.10:g.19987763G>A , CM000670.1:g.19987763G>A	GRCh37
NC_000008.9:g.20032043G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949563.1:n.3408+333G>A
XR_949563.2:n.3400+333G>A