Canonical Allele Identifier: CA857924172
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1445486657

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261811_103261812dup , CM000671.2:g.103261811_103261812dup GRCh38
NC_000009.11:g.106024093_106024094dup , CM000671.1:g.106024093_106024094dup GRCh37
NC_000009.10:g.105063914_105063915dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2715_771+2716dup