Canonical Allele Identifier: CA1693197789
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845383_20845389delinsGGATTCT , CM000669.2:g.20845383_20845389delinsGGATTCT GRCh38
NC_000007.13:g.20885002_20885008delinsGGATTCT , CM000669.1:g.20885002_20885008delinsGGATTCT GRCh37
NC_000007.12:g.20851527_20851533delinsGGATTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9879_74+9885delinsGGATTCT