Canonical Allele Identifier: CA1693197793
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845389T= , CM000669.2:g.20845389T= GRCh38
NC_000007.13:g.20885008T= , CM000669.1:g.20885008T= GRCh37
NC_000007.12:g.20851533T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9885T=