Canonical Allele Identifier: CA860367888

Gene:

Linked Data

• dbSNP Id: rs1311891836
• MyVariant Identifiers: chr9:g.132339110G>T (hg19) ; chr9:g.129576831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576831G>T , CM000671.2:g.129576831G>T	GRCh38
NC_000009.11:g.132339110G>T , CM000671.1:g.132339110G>T	GRCh37
NC_000009.10:g.131378931G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1233G>T