Canonical Allele Identifier: CA693367732
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1405887636
gnomAD v3: 12-91111727-C-G
gnomAD v4: 12-91111727-C-G
MyVariant Identifiers: chr12:g.91505504C>G (hg19) chr12:g.91111727C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111727C>G , CM000674.2:g.91111727C>G GRCh38
NC_000012.11:g.91505504C>G , CM000674.1:g.91505504C>G GRCh37
NC_000012.10:g.90029635C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-351G>C ENSP00000266718.4:n.-351G>C
NM_002345.3:c.-351G>C NP_002336.1:n.-351G>C
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