Canonical Allele Identifier: CA2054318187
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1592662335

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107221A>C , CM000674.2:g.91107221A>C GRCh38
NC_000012.11:g.91500998A>C , CM000674.1:g.91500998A>C GRCh37
NC_000012.10:g.90025129A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+897T>G MANE Select ENSP00000266718.4:n.862+897T>G
ENST00000266718.4:c.862+897T>G ENSP00000266718.4:n.862+897T>G
ENST00000546642.1:n.612+897T>G
ENST00000548071.1:n.255+897T>G
NM_002345.3:c.862+897T>G NP_002336.1:n.862+897T>G
NM_002345.4:c.862+897T>G MANE Select NP_002336.1:n.862+897T>G