Canonical Allele Identifier: CA1869205420
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261854_103261855delinsAG , CM000671.2:g.103261854_103261855delinsAG GRCh38
NC_000009.11:g.106024136_106024137delinsAG , CM000671.1:g.106024136_106024137delinsAG GRCh37
NC_000009.10:g.105063957_105063958delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2669_771+2670delinsCT