Canonical Allele Identifier: CA1693234731
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954785_20954787delinsTTA , CM000669.2:g.20954785_20954787delinsTTA GRCh38
NC_000007.13:g.20994404_20994406delinsTTA , CM000669.1:g.20994404_20994406delinsTTA GRCh37
NC_000007.12:g.20960929_20960931delinsTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66083_152-66081delinsTTA