Canonical Allele Identifier: CA950430431
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880107751
gnomAD v3: 12-91107472-T-A
gnomAD v4: 12-91107472-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107472T>A , CM000674.2:g.91107472T>A GRCh38
NC_000012.11:g.91501249T>A , CM000674.1:g.91501249T>A GRCh37
NC_000012.10:g.90025380T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+646A>T MANE Select ENSP00000266718.4:n.862+646A>T
ENST00000266718.4:c.862+646A>T ENSP00000266718.4:n.862+646A>T
ENST00000546642.1:n.612+646A>T
ENST00000548071.1:n.255+646A>T
NM_002345.3:c.862+646A>T NP_002336.1:n.862+646A>T
NM_002345.4:c.862+646A>T MANE Select NP_002336.1:n.862+646A>T
Search 100 bp 5'
Search 100 bp 3'