Canonical Allele Identifier: CA950429032
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880058800
gnomAD v3: 12-91107191-A-T
gnomAD v4: 12-91107191-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107191A>T , CM000674.2:g.91107191A>T GRCh38
NC_000012.11:g.91500968A>T , CM000674.1:g.91500968A>T GRCh37
NC_000012.10:g.90025099A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+927T>A MANE Select ENSP00000266718.4:n.862+927T>A
ENST00000266718.4:c.862+927T>A ENSP00000266718.4:n.862+927T>A
ENST00000546642.1:n.612+927T>A
ENST00000548071.1:n.255+927T>A
NM_002345.3:c.862+927T>A NP_002336.1:n.862+927T>A
NM_002345.4:c.862+927T>A MANE Select NP_002336.1:n.862+927T>A
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