Canonical Allele Identifier: CA112916442

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1296307G>C , CM000667.2:g.1296307G>C	GRCh38
NC_000005.9:g.1296422G>C , CM000667.1:g.1296422G>C	GRCh37
NC_000005.8:g.1349422G>C	NCBI36
NG_009265.1:g.3741C>G , LRG_343:g.3741C>G