Canonical Allele Identifier: CA2054320757
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880209646
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111766G>A , CM000674.2:g.91111766G>A GRCh38
NC_000012.11:g.91505543G>A , CM000674.1:g.91505543G>A GRCh37
NC_000012.10:g.90029674G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-390C>T ENSP00000266718.4:n.-390C>T
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