Canonical Allele Identifier: CA1869205363
Gene: LINC01492 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261733_103261734delinsTC , CM000671.2:g.103261733_103261734delinsTC GRCh38
NC_000009.11:g.106024015_106024016delinsTC , CM000671.1:g.106024015_106024016delinsTC GRCh37
NC_000009.10:g.105063836_105063837delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2790_771+2791delinsGA
Search 100 bp 5'
Search 100 bp 3'