Canonical Allele Identifier: CA1869205428
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261872_103261877delinsTAAAAC , CM000671.2:g.103261872_103261877delinsTAAAAC GRCh38
NC_000009.11:g.106024154_106024159delinsTAAAAC , CM000671.1:g.106024154_106024159delinsTAAAAC GRCh37
NC_000009.10:g.105063975_105063980delinsTAAAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2647_771+2652delinsGTTTTA