Canonical Allele Identifier: CA860367925

Gene:

Linked Data

• dbSNP Id: rs1212570787
• gnomAD v3: 9-129576893-G-C
• gnomAD v4: 9-129576893-G-C
• MyVariant Identifiers: chr9:g.132339172G>C (hg19) ; chr9:g.129576893G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576893G>C , CM000671.2:g.129576893G>C	GRCh38
NC_000009.11:g.132339172G>C , CM000671.1:g.132339172G>C	GRCh37
NC_000009.10:g.131378993G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1295G>C