Canonical Allele Identifier: CA734389766

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2581777C>G , CM000663.2:g.2581777C>G	GRCh38
NC_000001.10:g.2513216C>G , CM000663.1:g.2513216C>G	GRCh37
NC_000001.9:g.2503076C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121638.1:n.162+127C>G