Canonical Allele Identifier: CA117707983

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40401428T>A , CM000667.2:g.40401428T>A	GRCh38
NC_000005.9:g.40401530T>A , CM000667.1:g.40401530T>A	GRCh37
NC_000005.8:g.40437287T>A	NCBI36