Canonical Allele Identifier: CA2054320758
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111768G= , CM000674.2:g.91111768G= GRCh38
NC_000012.11:g.91505545G= , CM000674.1:g.91505545G= GRCh37
NC_000012.10:g.90029676G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-392C= ENSP00000266718.4:n.-392C=