Canonical Allele Identifier: CA2054320689
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111637G= , CM000674.2:g.91111637G= GRCh38
NC_000012.11:g.91505414G= , CM000674.1:g.91505414G= GRCh37
NC_000012.10:g.90029545G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-261C= ENSP00000266718.4:n.-261C=
NM_002345.3:c.-261C= NP_002336.1:n.-261C=