Canonical Allele Identifier: CA586058603

Gene:

Linked Data

• dbSNP Id: rs1216655901
• gnomAD v2: 9-1787626-A-G
• gnomAD v3: 9-1787626-A-G
• gnomAD v4: 9-1787626-A-G
• MyVariant Identifiers: chr9:g.1787626A>G (hg19) ; chr9:g.1787626A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787626A>G , CM000671.2:g.1787626A>G	GRCh38
NC_000009.11:g.1787626A>G , CM000671.1:g.1787626A>G	GRCh37
NC_000009.10:g.1777626A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001746599.1:n.142+68714A>G