Canonical Allele Identifier: CA2054320767
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111779T= , CM000674.2:g.91111779T= GRCh38
NC_000012.11:g.91505556T= , CM000674.1:g.91505556T= GRCh37
NC_000012.10:g.90029687T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-403A= ENSP00000266718.4:n.-403A=