Canonical Allele Identifier: CA1869205452
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261923_103261924delinsTA , CM000671.2:g.103261923_103261924delinsTA GRCh38
NC_000009.11:g.106024205_106024206delinsTA , CM000671.1:g.106024205_106024206delinsTA GRCh37
NC_000009.10:g.105064026_105064027delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2600_771+2601delinsTA