Canonical Allele Identifier: CA855697476

Gene:

Linked Data

• dbSNP Id: rs1433566474
• gnomAD v3: 8-79191109-G-A
• gnomAD v4: 8-79191109-G-A
• MyVariant Identifiers: chr8:g.80103344G>A (hg19) ; chr8:g.79191109G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191109G>A , CM000670.2:g.79191109G>A	GRCh38
NC_000008.10:g.80103344G>A , CM000670.1:g.80103344G>A	GRCh37
NC_000008.9:g.80265899G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745720.1:n.105+738G>A