Canonical Allele Identifier: CA783226050

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106946dup , CM000681.2:g.1106946dup	GRCh38
NC_000019.9:g.1106945dup , CM000681.1:g.1106945dup	GRCh37
NC_000019.8:g.1057945dup	NCBI36
NG_050621.1:g.8021dup