Canonical Allele Identifier: CA2054320659
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111555C= , CM000674.2:g.91111555C= GRCh38
NC_000012.11:g.91505332C= , CM000674.1:g.91505332C= GRCh37
NC_000012.10:g.90029463C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.4:c.-179G= ENSP00000266718.4:n.-179G=
NM_002345.3:c.-179G= NP_002336.1:n.-179G=