Canonical Allele Identifier: CA123198073

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93151837T>A , CM000667.2:g.93151837T>A	GRCh38
NC_000005.9:g.92487543T>A , CM000667.1:g.92487543T>A	GRCh37
NC_000005.8:g.92513299T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948569.1:n.130-1931A>T
XR_948569.2:n.197-1931A>T