Canonical Allele Identifier: CA2620150282
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111643G>T , CM000674.2:g.91111643G>T GRCh38
NC_000012.11:g.91505420G>T , CM000674.1:g.91505420G>T GRCh37
NC_000012.10:g.90029551G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-267C>A ENSP00000266718.4:n.-267C>A
NM_002345.3:c.-267C>A NP_002336.1:n.-267C>A