Canonical Allele Identifier: CA2001397822

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932113_113932134delinsCTGTCACTGAAAAGCTCATCTT , CM000673.2:g.113932113_113932134delinsCTGTCACTGAAAAGCTCATCTT	GRCh38
NC_000011.9:g.113802835_113802856delinsCTGTCACTGAAAAGCTCATCTT , CM000673.1:g.113802835_113802856delinsCTGTCACTGAAAAGCTCATCTT	GRCh37
NC_000011.8:g.113308045_113308066delinsCTGTCACTGAAAAGCTCATCTT	NCBI36
NG_011483.1:g.32247_32268delinsCTGTCACTGAAAAGCTCATCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT MANE Select	ENSP00000260191.2:n.369-176_369-155delinsCTGTCACTGAAAAGCTCATC...
ENST00000260191.7:c.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT	ENSP00000260191.2:n.369-176_369-155delinsCTGTCACTGAAAAGCTCATC...
ENST00000260191.6:c.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT	ENSP00000260191.2:n.369-176_369-155delinsCTGTCACTGAAAAGCTCATC...
ENST00000537778.5:c.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT	ENSP00000443118.1:n.336-176_336-155delinsCTGTCACTGAAAAGCTCATC...
ENST00000543092.1:c.155-176_155-155delinsCTGTCACTGAAAAGCTCATCTT
NM_006028.4:c.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT	NP_006019.1:n.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT
XM_011543063.1:c.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT	XP_011541365.1:n.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT
XM_011543064.1:c.168-176_168-155delinsCTGTCACTGAAAAGCTCATCTT	XP_011541366.1:n.168-176_168-155delinsCTGTCACTGAAAAGCTCATCTT
XM_011543065.1:c.162-176_162-155delinsCTGTCACTGAAAAGCTCATCTT	XP_011541367.1:n.162-176_162-155delinsCTGTCACTGAAAAGCTCATCTT
XM_011543066.1:c.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT	XP_011541368.1:n.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT
NM_001363563.1:c.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT	NP_001350492.1:n.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT
XM_017018552.2:c.162-176_162-155delinsCTGTCACTGAAAAGCTCATCTT	XP_016874041.1:n.162-176_162-155delinsCTGTCACTGAAAAGCTCATCTT
XM_024448767.1:c.75-176_75-155delinsCTGTCACTGAAAAGCTCATCTT	XP_024304535.1:n.75-176_75-155delinsCTGTCACTGAAAAGCTCATCTT
XR_001748034.2:n.620-176_620-155delinsCTGTCACTGAAAAGCTCATCTT
NM_001363563.2:c.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT	NP_001350492.1:n.336-176_336-155delinsCTGTCACTGAAAAGCTCATCTT
NM_006028.5:c.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT MANE Select	NP_006019.1:n.369-176_369-155delinsCTGTCACTGAAAAGCTCATCTT