Canonical Allele Identifier: CA897335771

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114123166G>C , CM000665.2:g.114123166G>C	GRCh38
NC_000003.11:g.113842013G>C , CM000665.1:g.113842013G>C	GRCh37
NC_000003.10:g.115324703G>C	NCBI36