Canonical Allele Identifier: CA2054320596
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880201766
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111454A>T , CM000674.2:g.91111454A>T GRCh38
NC_000012.11:g.91505231A>T , CM000674.1:g.91505231A>T GRCh37
NC_000012.10:g.90029362A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-78T>A MANE Select ENSP00000266718.4:n.-78T>A
ENST00000266718.4:c.-78T>A ENSP00000266718.4:n.-78T>A
ENST00000548071.1:n.33T>A
NM_002345.3:c.-78T>A NP_002336.1:n.-78T>A
NM_002345.4:c.-78T>A MANE Select NP_002336.1:n.-78T>A
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