Canonical Allele Identifier: CA1099137353
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781822682

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845385_20845390del , CM000669.2:g.20845385_20845390del GRCh38
NC_000007.13:g.20885004_20885009del , CM000669.1:g.20885004_20885009del GRCh37
NC_000007.12:g.20851529_20851534del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9881_74+9886del