Canonical Allele Identifier: CA241230519
Gene: LUM HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2268578

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107421A>G , CM000674.2:g.91107421A>G GRCh38
NC_000012.11:g.91501198A>G , CM000674.1:g.91501198A>G GRCh37
NC_000012.10:g.90025329A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002345.3:c.862+697T>C VV NP_002336.1:p.=
NM_002345.4:c.862+697T>C VV MANE Preferred NP_002336.1:p.=
ENST00000266718.4:c.862+697T>C ENSP00000266718.4:p.=
ENST00000546642.1:n.612+697T>C
ENST00000548071.1:n.255+697T>C