Canonical Allele Identifier: CA1099137347
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781822560

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845377_20845381del , CM000669.2:g.20845377_20845381del GRCh38
NC_000007.13:g.20884996_20885000del , CM000669.1:g.20884996_20885000del GRCh37
NC_000007.12:g.20851521_20851525del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9873_74+9877del