Canonical Allele Identifier: CA2054320760
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1788702242

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111769A>C , CM000674.2:g.91111769A>C GRCh38
NC_000012.11:g.91505546A>C , CM000674.1:g.91505546A>C GRCh37
NC_000012.10:g.90029677A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-393T>G ENSP00000266718.4:n.-393T>G