Canonical Allele Identifier: CA191701696

Gene:

Linked Data

• dbSNP Id: rs1031639661
• gnomAD v3: 9-25551336-A-C
• gnomAD v4: 9-25551336-A-C
• MyVariant Identifiers: chr9:g.25551334A>C (hg19) ; chr9:g.25551336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551336A>C , CM000671.2:g.25551336A>C	GRCh38
NC_000009.11:g.25551334A>C , CM000671.1:g.25551334A>C	GRCh37
NC_000009.10:g.25541334A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-764T>G
XR_929525.2:n.674-764T>G