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Human (GRCh38.p14)
Description

lamin B2 [Source:HGNC Symbol;Acc:HGNC:6638]

Gene Synonyms

LMN2

Location

Chromosome 19: 2,427,638-2,456,959 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 6 transcripts (splice variants), 187 orthologues, 68 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000325327.4LMNB2-2014634620aaENSP00000327054.3
 
Protein coding
CCDS12090Q03252 NM_032737.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000475819.1LMNB2-202885No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000527409.1LMNB2-204838No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000532465.1LMNB2-205769No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000534495.1LMNB2-206491No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000490554.5LMNB2-203689No protein-
 
Retained intron
--TSL:2