Canonical Allele Identifier: CA917959776
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1554304533

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954791del , CM000669.2:g.20954791del GRCh38
NC_000007.13:g.20994410del , CM000669.1:g.20994410del GRCh37
NC_000007.12:g.20960935del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66077del