Canonical Allele Identifier: CA950430423
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880107360

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107454A>G , CM000674.2:g.91107454A>G GRCh38
NC_000012.11:g.91501231A>G , CM000674.1:g.91501231A>G GRCh37
NC_000012.10:g.90025362A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+664T>C MANE Select ENSP00000266718.4:n.862+664T>C
ENST00000266718.4:c.862+664T>C ENSP00000266718.4:n.862+664T>C
ENST00000546642.1:n.612+664T>C
ENST00000548071.1:n.255+664T>C
NM_002345.3:c.862+664T>C NP_002336.1:n.862+664T>C
NM_002345.4:c.862+664T>C MANE Select NP_002336.1:n.862+664T>C