Canonical Allele Identifier: CA918523336
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1587822243

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262108del , CM000671.2:g.103262108del GRCh38
NC_000009.11:g.106024390del , CM000671.1:g.106024390del GRCh37
NC_000009.10:g.105064211del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2418del