Canonical Allele Identifier: CA950428830
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1592662268
gnomAD v3: 12-91107132-T-A
gnomAD v4: 12-91107132-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107132T>A , CM000674.2:g.91107132T>A GRCh38
NC_000012.11:g.91500909T>A , CM000674.1:g.91500909T>A GRCh37
NC_000012.10:g.90025040T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+986A>T MANE Select ENSP00000266718.4:n.862+986A>T
ENST00000266718.4:c.862+986A>T ENSP00000266718.4:n.862+986A>T
ENST00000546642.1:n.612+986A>T
ENST00000548071.1:n.255+986A>T
NM_002345.3:c.862+986A>T NP_002336.1:n.862+986A>T
NM_002345.4:c.862+986A>T MANE Select NP_002336.1:n.862+986A>T
Search 100 bp 5'
Search 100 bp 3'