Canonical Allele Identifier: CA1254163835
Gene: LINC01122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.59055456T= , CM000664.2:g.59055456T= GRCh38
NC_000002.11:g.59282591T= , CM000664.1:g.59282591T= GRCh37
NC_000002.10:g.59136095T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.1273-3105T=