Canonical Allele Identifier: CA950406973
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1650596054
gnomAD v3: 12-91111636-T-C
gnomAD v4: 12-91111636-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111636T>C , CM000674.2:g.91111636T>C GRCh38
NC_000012.11:g.91505413T>C , CM000674.1:g.91505413T>C GRCh37
NC_000012.10:g.90029544T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-260A>G ENSP00000266718.4:n.-260A>G
NM_002345.3:c.-260A>G NP_002336.1:n.-260A>G
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