Canonical Allele Identifier: CA1254043235
Gene: LINC01122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58809766C= , CM000664.2:g.58809766C= GRCh38
NC_000002.11:g.59036901C= , CM000664.1:g.59036901C= GRCh37
NC_000002.10:g.58890405C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-40664C=