Canonical Allele Identifier: CA2600912205
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1485077335
gnomAD v3: 12-91111777-T-G
gnomAD v4: 12-91111777-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111777T>G , CM000674.2:g.91111777T>G GRCh38
NC_000012.11:g.91505554T>G , CM000674.1:g.91505554T>G GRCh37
NC_000012.10:g.90029685T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-401A>C ENSP00000266718.4:n.-401A>C
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