Canonical Allele Identifier: CA1693234677
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954720T= , CM000669.2:g.20954720T= GRCh38
NC_000007.13:g.20994339T= , CM000669.1:g.20994339T= GRCh37
NC_000007.12:g.20960864T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66148T=