Canonical Allele Identifier: CA950406978
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880207505

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111651A>C , CM000674.2:g.91111651A>C GRCh38
NC_000012.11:g.91505428A>C , CM000674.1:g.91505428A>C GRCh37
NC_000012.10:g.90029559A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-275T>G ENSP00000266718.4:n.-275T>G
NM_002345.3:c.-275T>G NP_002336.1:n.-275T>G