Canonical Allele Identifier: CA918523329
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1587822149

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261756_103261763dup , CM000671.2:g.103261756_103261763dup GRCh38
NC_000009.11:g.106024038_106024045dup , CM000671.1:g.106024038_106024045dup GRCh37
NC_000009.10:g.105063859_105063866dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2761_771+2768dup