Canonical Allele Identifier: CA858377615

Gene:

Linked Data

• dbSNP Id: rs1295240948
• gnomAD v3: 9-108092816-A-G
• gnomAD v4: 9-108092816-A-G
• MyVariant Identifiers: chr9:g.110855097A>G (hg19) ; chr9:g.108092816A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108092816A>G , CM000671.2:g.108092816A>G	GRCh38
NC_000009.11:g.110855097A>G , CM000671.1:g.110855097A>G	GRCh37
NC_000009.10:g.109894918A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930239.1:n.461-39522T>C
XR_001746881.1:n.668-39522T>C
XR_001746882.1:n.668-39522T>C