Canonical Allele Identifier: CA2001397927

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932321A= , CM000673.2:g.113932321A=	GRCh38
NC_000011.9:g.113803043A= , CM000673.1:g.113803043A=	GRCh37
NC_000011.8:g.113308253A=	NCBI36
NG_011483.1:g.32455A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.401A= MANE Select	ENSP00000260191.2:p.Tyr134=
ENST00000260191.7:c.401A=	ENSP00000260191.2:p.Tyr134=
ENST00000260191.6:c.401A=	ENSP00000260191.2:p.Tyr134=
ENST00000537778.5:c.368A=	ENSP00000443118.1:p.Tyr123=
ENST00000543092.1:c.187A=
NM_006028.4:c.401A=	NP_006019.1:p.Tyr134=
XM_011543063.1:c.368A=	XP_011541365.1:p.Tyr123=
XM_011543064.1:c.200A=	XP_011541366.1:p.Tyr67=
XM_011543065.1:c.194A=	XP_011541367.1:p.Tyr65=
XM_011543066.1:c.368A=	XP_011541368.1:p.Tyr123=
NM_001363563.1:c.368A=	NP_001350492.1:p.Tyr123=
XM_017018552.2:c.194A=	XP_016874041.1:p.Tyr65=
XM_024448767.1:c.107A=	XP_024304535.1:p.Tyr36=
XR_001748034.2:n.652A=
NM_001363563.2:c.368A=	NP_001350492.1:p.Tyr123=
NM_006028.5:c.401A= MANE Select	NP_006019.1:p.Tyr134=