Canonical Allele Identifier: CA950407020
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1029857275
gnomAD v3: 12-91111715-A-T
gnomAD v4: 12-91111715-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111715A>T , CM000674.2:g.91111715A>T GRCh38
NC_000012.11:g.91505492A>T , CM000674.1:g.91505492A>T GRCh37
NC_000012.10:g.90029623A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-339T>A ENSP00000266718.4:n.-339T>A
NM_002345.3:c.-339T>A NP_002336.1:n.-339T>A
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