Canonical Allele Identifier: CA2796947693
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107442A>T , CM000674.2:g.91107442A>T GRCh38
NC_000012.11:g.91501219A>T , CM000674.1:g.91501219A>T GRCh37
NC_000012.10:g.90025350A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+676T>A MANE Select ENSP00000266718.4:n.862+676T>A
ENST00000266718.4:c.862+676T>A ENSP00000266718.4:n.862+676T>A
ENST00000546642.1:n.612+676T>A
ENST00000548071.1:n.255+676T>A
NM_002345.3:c.862+676T>A NP_002336.1:n.862+676T>A
NM_002345.4:c.862+676T>A MANE Select NP_002336.1:n.862+676T>A
Search 100 bp 5'
Search 100 bp 3'