Canonical Allele Identifier: CA1591627478
Gene: LINC01933 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151964997G>T , CM000667.2:g.151964997G>T GRCh38
NC_000005.9:g.151344558G>T , CM000667.1:g.151344558G>T GRCh37
NC_000005.8:g.151324751G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109876.1:n.57+6043G>T