Canonical Allele Identifier: CA693367743
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1199738232

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111742G>C , CM000674.2:g.91111742G>C GRCh38
NC_000012.11:g.91505519G>C , CM000674.1:g.91505519G>C GRCh37
NC_000012.10:g.90029650G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-366C>G ENSP00000266718.4:n.-366C>G
NM_002345.3:c.-366C>G NP_002336.1:n.-366C>G