Canonical Allele Identifier: CA2796947790
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111736A>G , CM000674.2:g.91111736A>G GRCh38
NC_000012.11:g.91505513A>G , CM000674.1:g.91505513A>G GRCh37
NC_000012.10:g.90029644A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-360T>C ENSP00000266718.4:n.-360T>C
NM_002345.3:c.-360T>C NP_002336.1:n.-360T>C