Canonical Allele Identifier: CA693367699
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1261831285

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111639A>G , CM000674.2:g.91111639A>G GRCh38
NC_000012.11:g.91505416A>G , CM000674.1:g.91505416A>G GRCh37
NC_000012.10:g.90029547A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-263T>C ENSP00000266718.4:n.-263T>C
NM_002345.3:c.-263T>C NP_002336.1:n.-263T>C