Canonical Allele Identifier: CA1693234728
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954780G= , CM000669.2:g.20954780G= GRCh38
NC_000007.13:g.20994399G= , CM000669.1:g.20994399G= GRCh37
NC_000007.12:g.20960924G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66088G=