Canonical Allele Identifier: CA241233971
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs937390527

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111633A>G , CM000674.2:g.91111633A>G GRCh38
NC_000012.11:g.91505410A>G , CM000674.1:g.91505410A>G GRCh37
NC_000012.10:g.90029541A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-257T>C ENSP00000266718.4:n.-257T>C
NM_002345.3:c.-257T>C NP_002336.1:n.-257T>C