Canonical Allele Identifier: CA12885613

Gene: LINC01151

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122693916G>A , CM000670.2:g.122693916G>A	GRCh38
NC_000008.10:g.123706155G>A , CM000670.1:g.123706155G>A	GRCh37
NC_000008.9:g.123775336G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126348.1:n.191C>T