Canonical Allele Identifier: CA2054320705
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111664T= , CM000674.2:g.91111664T= GRCh38
NC_000012.11:g.91505441T= , CM000674.1:g.91505441T= GRCh37
NC_000012.10:g.90029572T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-288A= ENSP00000266718.4:n.-288A=
NM_002345.3:c.-288A= NP_002336.1:n.-288A=