Canonical Allele Identifier: CA2054320649
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1491312695
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111533_91111534insGGT , CM000674.2:g.91111533_91111534insGGT GRCh38
NC_000012.11:g.91505310_91505311insGGT , CM000674.1:g.91505310_91505311insGGT GRCh37
NC_000012.10:g.90029441_90029442insGGT NCBI36

Transcript Alleles

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