Canonical Allele Identifier: CA606704126
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1555188945
gnomAD v2: 12-91505309-G-GGC
gnomAD v3: 12-91111532-G-GGC
gnomAD v4: 12-91111532-G-GGC
MyVariant Identifiers: chr12:g.91505309_91505310insGC (hg19) chr12:g.91111532_91111533insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111533_91111534insCG , CM000674.2:g.91111533_91111534insCG GRCh38
NC_000012.11:g.91505310_91505311insCG , CM000674.1:g.91505310_91505311insCG GRCh37
NC_000012.10:g.90029441_90029442insCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-157_-156insGC ENSP00000266718.4:n.-157_-156insGC
NM_002345.3:c.-157_-156insGC NP_002336.1:n.-157_-156insGC
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