Canonical Allele Identifier: CA2001397957

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932382G= , CM000673.2:g.113932382G=	GRCh38
NC_000011.9:g.113803104G= , CM000673.1:g.113803104G=	GRCh37
NC_000011.8:g.113308314G=	NCBI36
NG_011483.1:g.32516G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.462G= MANE Select	ENSP00000260191.2:p.Ala154=
ENST00000260191.7:c.462G=	ENSP00000260191.2:p.Ala154=
ENST00000260191.6:c.462G=	ENSP00000260191.2:p.Ala154=
ENST00000537778.5:c.429G=	ENSP00000443118.1:p.Ala143=
ENST00000543092.1:c.248G=
NM_006028.4:c.462G=	NP_006019.1:p.Ala154=
XM_011543063.1:c.429G=	XP_011541365.1:p.Ala143=
XM_011543064.1:c.261G=	XP_011541366.1:p.Ala87=
XM_011543065.1:c.255G=	XP_011541367.1:p.Ala85=
XM_011543066.1:c.429G=	XP_011541368.1:p.Ala143=
NM_001363563.1:c.429G=	NP_001350492.1:p.Ala143=
XM_017018552.2:c.255G=	XP_016874041.1:p.Ala85=
XM_024448767.1:c.168G=	XP_024304535.1:p.Ala56=
XR_001748034.2:n.713G=
NM_001363563.2:c.429G=	NP_001350492.1:p.Ala143=
NM_006028.5:c.462G= MANE Select	NP_006019.1:p.Ala154=