Canonical Allele Identifier: CA606704125
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1555188945
gnomAD v2: 12-91505309-G-GGA
MyVariant Identifiers: chr12:g.91505309_91505310insGA (hg19) chr12:g.91111532_91111533insGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111533_91111534insAG , CM000674.2:g.91111533_91111534insAG GRCh38
NC_000012.11:g.91505310_91505311insAG , CM000674.1:g.91505310_91505311insAG GRCh37
NC_000012.10:g.90029441_90029442insAG NCBI36

Transcript Alleles

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