Canonical Allele Identifier: CA1253945374
Gene: LINC01122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58606358A>C , CM000664.2:g.58606358A>C GRCh38
NC_000002.11:g.58833493A>C , CM000664.1:g.58833493A>C GRCh37
NC_000002.10:g.58686997A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.186-50292A>C