Canonical Allele Identifier: CA1869205488
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262011_103262017delinsGTAAAAC , CM000671.2:g.103262011_103262017delinsGTAAAAC GRCh38
NC_000009.11:g.106024293_106024299delinsGTAAAAC , CM000671.1:g.106024293_106024299delinsGTAAAAC GRCh37
NC_000009.10:g.105064114_105064120delinsGTAAAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2507_771+2513delinsGTTTTAC