Canonical Allele Identifier: CA1869205405
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261814_103261816delinsTGA , CM000671.2:g.103261814_103261816delinsTGA GRCh38
NC_000009.11:g.106024096_106024098delinsTGA , CM000671.1:g.106024096_106024098delinsTGA GRCh37
NC_000009.10:g.105063917_105063919delinsTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2708_771+2710delinsTCA