Canonical Allele Identifier: CA2054320778
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111804T= , CM000674.2:g.91111804T= GRCh38
NC_000012.11:g.91505581T= , CM000674.1:g.91505581T= GRCh37
NC_000012.10:g.90029712T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-428A= ENSP00000266718.4:n.-428A=