Canonical Allele Identifier: CA1254163837
Gene: LINC01122 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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