Canonical Allele Identifier: CA693367720
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1296460670
MyVariant Identifiers: chr12:g.91505475_91505478del (hg19) chr12:g.91111698_91111701del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111700_91111703del , CM000674.2:g.91111700_91111703del GRCh38
NC_000012.11:g.91505477_91505480del , CM000674.1:g.91505477_91505480del GRCh37
NC_000012.10:g.90029608_90029611del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-325_-322del ENSP00000266718.4:n.-325_-322del
NM_002345.3:c.-325_-322del NP_002336.1:n.-325_-322del
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