Canonical Allele Identifier: CA1693197782
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845375_20845380delinsTTGGAA , CM000669.2:g.20845375_20845380delinsTTGGAA GRCh38
NC_000007.13:g.20884994_20884999delinsTTGGAA , CM000669.1:g.20884994_20884999delinsTTGGAA GRCh37
NC_000007.12:g.20851519_20851524delinsTTGGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9871_74+9876delinsTTGGAA