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Human (GRCh38.p14)
Description

Smith-Magenis syndrome chromosome region, candidate 2 [Source:HGNC Symbol;Acc:HGNC:17914]

Location

Chromosome 17: 17,674,026-17,677,688 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 1 transcript (splice variant).

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000456090.2SMCR2-201564No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:2