Canonical Allele Identifier: CA1693197820
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845414T= , CM000669.2:g.20845414T= GRCh38
NC_000007.13:g.20885033T= , CM000669.1:g.20885033T= GRCh37
NC_000007.12:g.20851558T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9910T=