Canonical Allele Identifier: CA2054320720
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880208240

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111691_91111692del , CM000674.2:g.91111691_91111692del GRCh38
NC_000012.11:g.91505468_91505469del , CM000674.1:g.91505468_91505469del GRCh37
NC_000012.10:g.90029599_90029600del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-314_-313del ENSP00000266718.4:n.-314_-313del
NM_002345.3:c.-314_-313del NP_002336.1:n.-314_-313del