Canonical Allele Identifier: CA2054320741
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs543724006

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111720T>A , CM000674.2:g.91111720T>A GRCh38
NC_000012.11:g.91505497T>A , CM000674.1:g.91505497T>A GRCh37
NC_000012.10:g.90029628T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-344A>T ENSP00000266718.4:n.-344A>T
NM_002345.3:c.-344A>T NP_002336.1:n.-344A>T