Canonical Allele Identifier: CA200491708

Gene:

Linked Data

• dbSNP Id: rs75217434
• gnomAD v3: 9-129576858-G-T
• gnomAD v4: 9-129576858-G-T
• MyVariant Identifiers: chr9:g.132339137G>T (hg19) ; chr9:g.129576858G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576858G>T , CM000671.2:g.129576858G>T	GRCh38
NC_000009.11:g.132339137G>T , CM000671.1:g.132339137G>T	GRCh37
NC_000009.10:g.131378958G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1260G>T