Canonical Allele Identifier: CA2054320780
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1592664272

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111806T>G , CM000674.2:g.91111806T>G GRCh38
NC_000012.11:g.91505583T>G , CM000674.1:g.91505583T>G GRCh37
NC_000012.10:g.90029714T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-430A>C ENSP00000266718.4:n.-430A>C