Canonical Allele Identifier: CA16085296

Gene: LINC02774

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244013122G>T , CM000663.2:g.244013122G>T	GRCh38
NC_000001.10:g.244176424G>T , CM000663.1:g.244176424G>T	GRCh37
NC_000001.9:g.242243047G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033883.1:n.750+2202G>T