Canonical Allele Identifier: CA788191465

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141842417G>T , CM000666.2:g.141842417G>T	GRCh38
NC_000004.11:g.142763570G>T , CM000666.1:g.142763570G>T	GRCh37
NC_000004.10:g.142983020G>T	NCBI36