Canonical Allele Identifier: CA747163334

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14472592G>C , CM000683.2:g.14472592G>C	GRCh38
NC_000021.8:g.15844913G>C , CM000683.1:g.15844913G>C	GRCh37
NC_000021.7:g.14766784G>C	NCBI36