Canonical Allele Identifier: CA2054320647
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880205033

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111533_91111534insAGG , CM000674.2:g.91111533_91111534insAGG GRCh38
NC_000012.11:g.91505310_91505311insAGG , CM000674.1:g.91505310_91505311insAGG GRCh37
NC_000012.10:g.90029441_90029442insAGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.4:c.-156_-155insTCC ENSP00000266718.4:n.-156_-155insTCC
NM_002345.3:c.-156_-155insTCC NP_002336.1:n.-156_-155insTCC