Canonical Allele Identifier: CA860367916

Gene:

Linked Data

• dbSNP Id: rs1177436410
• MyVariant Identifiers: chr9:g.132339144C>A (hg19) ; chr9:g.129576865C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576865C>A , CM000671.2:g.129576865C>A	GRCh38
NC_000009.11:g.132339144C>A , CM000671.1:g.132339144C>A	GRCh37
NC_000009.10:g.131378965C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1267C>A