Canonical Allele Identifier: CA2054320739
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880208928
gnomAD v4: 12-91111719-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111719C>A , CM000674.2:g.91111719C>A GRCh38
NC_000012.11:g.91505496C>A , CM000674.1:g.91505496C>A GRCh37
NC_000012.10:g.90029627C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-343G>T ENSP00000266718.4:n.-343G>T
NM_002345.3:c.-343G>T NP_002336.1:n.-343G>T
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