Canonical Allele Identifier: CA586058581

Gene:

Linked Data

• dbSNP Id: rs928368589
• gnomAD v2: 9-1787446-T-A
• gnomAD v3: 9-1787446-T-A
• gnomAD v4: 9-1787446-T-A
• MyVariant Identifiers: chr9:g.1787446T>A (hg19) ; chr9:g.1787446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787446T>A , CM000671.2:g.1787446T>A	GRCh38
NC_000009.11:g.1787446T>A , CM000671.1:g.1787446T>A	GRCh37
NC_000009.10:g.1777446T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746599.1:n.142+68534T>A