Canonical Allele Identifier: CA200491623

Gene:

Linked Data

• dbSNP Id: rs1046698481
• gnomAD v3: 9-129576761-G-A
• gnomAD v4: 9-129576761-G-A
• MyVariant Identifiers: chr9:g.132339040G>A (hg19) ; chr9:g.129576761G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576761G>A , CM000671.2:g.129576761G>A	GRCh38
NC_000009.11:g.132339040G>A , CM000671.1:g.132339040G>A	GRCh37
NC_000009.10:g.131378861G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930390.1:n.182+1163G>A