Canonical Allele Identifier: CA200491559

Gene:

Linked Data

• dbSNP Id: rs531104609
• gnomAD v2: 9-132338985-C-T
• gnomAD v3: 9-129576706-C-T
• gnomAD v4: 9-129576706-C-T
• MyVariant Identifiers: chr9:g.132338985C>T (hg19) ; chr9:g.129576706C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576706C>T , CM000671.2:g.129576706C>T	GRCh38
NC_000009.11:g.132338985C>T , CM000671.1:g.132338985C>T	GRCh37
NC_000009.10:g.131378806C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1108C>T