Canonical Allele Identifier: CA1869205431
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261873_103261877delinsAAAAC , CM000671.2:g.103261873_103261877delinsAAAAC GRCh38
NC_000009.11:g.106024155_106024159delinsAAAAC , CM000671.1:g.106024155_106024159delinsAAAAC GRCh37
NC_000009.10:g.105063976_105063980delinsAAAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2647_771+2651delinsGTTTT