Canonical Allele Identifier: CA241233882
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1491312695
gnomAD v3: 12-91111533-G-GGT
gnomAD v4: 12-91111533-G-GGT
MyVariant Identifiers: chr12:g.91505310_91505311insGT (hg19) chr12:g.91111533_91111534insGT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111533_91111534insGT , CM000674.2:g.91111533_91111534insGT GRCh38
NC_000012.11:g.91505310_91505311insGT , CM000674.1:g.91505310_91505311insGT GRCh37
NC_000012.10:g.90029441_90029442insGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-158_-157insAC ENSP00000266718.4:n.-158_-157insAC
NM_002345.3:c.-158_-157insAC NP_002336.1:n.-158_-157insAC
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