Canonical Allele Identifier: CA2054320655
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111541A= , CM000674.2:g.91111541A= GRCh38
NC_000012.11:g.91505318A= , CM000674.1:g.91505318A= GRCh37
NC_000012.10:g.90029449A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-165T= ENSP00000266718.4:n.-165T=
NM_002345.3:c.-165T= NP_002336.1:n.-165T=