Canonical Allele Identifier: CA741300850

Gene: LINC01722

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.12893937T>A , CM000682.2:g.12893937T>A	GRCh38
NC_000020.10:g.12874585T>A , CM000682.1:g.12874585T>A	GRCh37
NC_000020.9:g.12822585T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109868.1:n.1669+410A>T