Canonical Allele Identifier: CA1254061506
Gene: LINC01122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58845834C= , CM000664.2:g.58845834C= GRCh38
NC_000002.11:g.59072969C= , CM000664.1:g.59072969C= GRCh37
NC_000002.10:g.58926473C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-4596C=