Canonical Allele Identifier: CA801257921

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.104872127T>C , CM000667.2:g.104872127T>C	GRCh38
NC_000005.9:g.104207828T>C , CM000667.1:g.104207828T>C	GRCh37
NC_000005.8:g.104235727T>C	NCBI36