Canonical Allele Identifier: CA311522251

Gene: LINC01428

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.7199409T>A , CM000682.2:g.7199409T>A	GRCh38
NC_000020.10:g.7180056T>A , CM000682.1:g.7180056T>A	GRCh37
NC_000020.9:g.7128056T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110609.1:n.165-10842A>T