Canonical Allele Identifier: CA2054320737
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880208887

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111718G>C , CM000674.2:g.91111718G>C GRCh38
NC_000012.11:g.91505495G>C , CM000674.1:g.91505495G>C GRCh37
NC_000012.10:g.90029626G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-342C>G ENSP00000266718.4:n.-342C>G
NM_002345.3:c.-342C>G NP_002336.1:n.-342C>G