Canonical Allele Identifier: CA189884014

Gene:

Linked Data

• dbSNP Id: rs760228022
• MyVariant Identifiers: chr9:g.12108933G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.12108933G>T , CM000671.2:g.12108933G>T	GRCh38
NC_000009.11:g.12108933G>T , CM000671.1:g.12108933G>T	GRCh37
NC_000009.10:g.12098933G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929481.1:n.166+7888C>A
XR_929482.1:n.260+7888C>A
XR_929481.2:n.166+7888C>A
XR_929482.2:n.260+7888C>A