Canonical Allele Identifier: CA653217540
Gene: LINC01492 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261938_103261939insC , CM000671.2:g.103261938_103261939insC GRCh38
NC_000009.11:g.106024220_106024221insC , CM000671.1:g.106024220_106024221insC GRCh37
NC_000009.10:g.105064041_105064042insC NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2585_771+2586insG