Canonical Allele Identifier: CA950429009
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs2121046066

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107184A>G , CM000674.2:g.91107184A>G GRCh38
NC_000012.11:g.91500961A>G , CM000674.1:g.91500961A>G GRCh37
NC_000012.10:g.90025092A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+934T>C MANE Select ENSP00000266718.4:n.862+934T>C
ENST00000266718.4:c.862+934T>C ENSP00000266718.4:n.862+934T>C
ENST00000546642.1:n.612+934T>C
ENST00000548071.1:n.255+934T>C
NM_002345.3:c.862+934T>C NP_002336.1:n.862+934T>C
NM_002345.4:c.862+934T>C MANE Select NP_002336.1:n.862+934T>C