Canonical Allele Identifier: CA624096219

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85927956G>T , CM000678.2:g.85927956G>T	GRCh38
NC_000016.9:g.85961562G>T , CM000678.1:g.85961562G>T	GRCh37
NC_000016.8:g.84519063G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933852.1:n.465+1472G>T
XR_933853.1:n.465+1472G>T