Canonical Allele Identifier: CA2054320717
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880208151

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111679T>C , CM000674.2:g.91111679T>C GRCh38
NC_000012.11:g.91505456T>C , CM000674.1:g.91505456T>C GRCh37
NC_000012.10:g.90029587T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-303A>G ENSP00000266718.4:n.-303A>G
NM_002345.3:c.-303A>G NP_002336.1:n.-303A>G