Canonical Allele Identifier: CA1693234717
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783252886

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954772G>A , CM000669.2:g.20954772G>A GRCh38
NC_000007.13:g.20994391G>A , CM000669.1:g.20994391G>A GRCh37
NC_000007.12:g.20960916G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66096G>A