Canonical Allele Identifier: CA1869205462
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261939_103261940delinsAG , CM000671.2:g.103261939_103261940delinsAG GRCh38
NC_000009.11:g.106024221_106024222delinsAG , CM000671.1:g.106024221_106024222delinsAG GRCh37
NC_000009.10:g.105064042_105064043delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2584_771+2585delinsCT