Canonical Allele Identifier: CA191701684

Gene:

Linked Data

• dbSNP Id: rs886371119
• gnomAD v3: 9-25551235-T-C
• gnomAD v4: 9-25551235-T-C
• MyVariant Identifiers: chr9:g.25551233T>C (hg19) ; chr9:g.25551235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551235T>C , CM000671.2:g.25551235T>C	GRCh38
NC_000009.11:g.25551233T>C , CM000671.1:g.25551233T>C	GRCh37
NC_000009.10:g.25541233T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-663A>G
XR_929525.2:n.674-663A>G