Canonical Allele Identifier: CA904067915

Gene: LINC01991

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187969286A>T , CM000665.2:g.187969286A>T	GRCh38
NC_000003.11:g.187687074A>T , CM000665.1:g.187687074A>T	GRCh37
NC_000003.10:g.189169768A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924815.1:n.97-2077T>A
NR_135537.1:n.83-2077T>A
NR_135538.1:n.83-2077T>A