Canonical Allele Identifier: CA12175104

Gene: LINC03000

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.165119891A>G , CM000667.2:g.165119891A>G	GRCh38
NC_000005.9:g.164546897A>G , CM000667.1:g.164546897A>G	GRCh37
NC_000005.8:g.164479475A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941179.1:n.357-51487A>G