Canonical Allele Identifier: CA197846259

Gene:

Linked Data

• dbSNP Id: rs971141802
• gnomAD v3: 9-108092726-T-C
• gnomAD v4: 9-108092726-T-C
• MyVariant Identifiers: chr9:g.110855007T>C (hg19) ; chr9:g.108092726T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108092726T>C , CM000671.2:g.108092726T>C	GRCh38
NC_000009.11:g.110855007T>C , CM000671.1:g.110855007T>C	GRCh37
NC_000009.10:g.109894828T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930239.1:n.461-39432A>G
XR_001746881.1:n.668-39432A>G
XR_001746882.1:n.668-39432A>G