Canonical Allele Identifier: CA2713980117
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs2128072852

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845429_20845431del , CM000669.2:g.20845429_20845431del GRCh38
NC_000007.13:g.20885048_20885050del , CM000669.1:g.20885048_20885050del GRCh37
NC_000007.12:g.20851573_20851575del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9925_74+9927del