Canonical Allele Identifier: CA2054320642
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111530G= , CM000674.2:g.91111530G= GRCh38
NC_000012.11:g.91505307G= , CM000674.1:g.91505307G= GRCh37
NC_000012.10:g.90029438G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-154C= ENSP00000266718.4:n.-154C=
NM_002345.3:c.-154C= NP_002336.1:n.-154C=