Canonical Allele Identifier: CA2054320657
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111544C= , CM000674.2:g.91111544C= GRCh38
NC_000012.11:g.91505321C= , CM000674.1:g.91505321C= GRCh37
NC_000012.10:g.90029452C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-168G= ENSP00000266718.4:n.-168G=
NM_002345.3:c.-168G= NP_002336.1:n.-168G=