Canonical Allele Identifier: CA436714525

Gene:

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169764551C>G , CM000665.2:g.169764551C>G	GRCh38
NC_000003.11:g.169482339C>G , CM000665.1:g.169482339C>G	GRCh37
NC_000003.10:g.170965033C>G	NCBI36
NG_016363.1:g.5510G>C , LRG_347:g.5510G>C