Canonical Allele Identifier: CA604317772

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28591708C>G , CM000674.2:g.28591708C>G	GRCh38
NC_000012.11:g.28744641C>G , CM000674.1:g.28744641C>G	GRCh37
NC_000012.10:g.28635908C>G	NCBI36