Canonical Allele Identifier: CA1254043211
Gene: LINC01122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58809720T= , CM000664.2:g.58809720T= GRCh38
NC_000002.11:g.59036855T= , CM000664.1:g.59036855T= GRCh37
NC_000002.10:g.58890359T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-40710T=