Canonical Allele Identifier: CA788220054

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141521637C>A , CM000666.2:g.141521637C>A	GRCh38
NC_000004.11:g.142442790C>A , CM000666.1:g.142442790C>A	GRCh37
NC_000004.10:g.142662240C>A	NCBI36