Canonical Allele Identifier: CA786417399

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122759915T>C , CM000666.2:g.122759915T>C	GRCh38
NC_000004.11:g.123681070T>C , CM000666.1:g.123681070T>C	GRCh37
NC_000004.10:g.123900520T>C	NCBI36