Canonical Allele Identifier: CA561687871

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.104872346T>A , CM000667.2:g.104872346T>A	GRCh38
NC_000005.9:g.104208047T>A , CM000667.1:g.104208047T>A	GRCh37
NC_000005.8:g.104235946T>A	NCBI36