Canonical Allele Identifier: CA2054320722
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs897306373

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111690T>G , CM000674.2:g.91111690T>G GRCh38
NC_000012.11:g.91505467T>G , CM000674.1:g.91505467T>G GRCh37
NC_000012.10:g.90029598T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-314A>C ENSP00000266718.4:n.-314A>C
NM_002345.3:c.-314A>C NP_002336.1:n.-314A>C