Canonical Allele Identifier: CA700906735

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75202132G>C , CM000675.2:g.75202132G>C	GRCh38
NC_000013.10:g.75776268G>C , CM000675.1:g.75776268G>C	GRCh37
NC_000013.9:g.74674269G>C	NCBI36