Canonical Allele Identifier: CA919144099
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs386377346

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111534_91111535del , CM000674.2:g.91111534_91111535del GRCh38
NC_000012.11:g.91505311_91505312del , CM000674.1:g.91505311_91505312del GRCh37
NC_000012.10:g.90029442_90029443del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-158_-157del ENSP00000266718.4:n.-158_-157del
NM_002345.3:c.-158_-157del NP_002336.1:n.-158_-157del