Canonical Allele Identifier: CA2001397958

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932383T= , CM000673.2:g.113932383T=	GRCh38
NC_000011.9:g.113803105T= , CM000673.1:g.113803105T=	GRCh37
NC_000011.8:g.113308315T=	NCBI36
NG_011483.1:g.32517T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.463T= MANE Select	ENSP00000260191.2:p.Cys155=
ENST00000260191.7:c.463T=	ENSP00000260191.2:p.Cys155=
ENST00000260191.6:c.463T=	ENSP00000260191.2:p.Cys155=
ENST00000537778.5:c.430T=	ENSP00000443118.1:p.Cys144=
ENST00000543092.1:c.249T=
NM_006028.4:c.463T=	NP_006019.1:p.Cys155=
XM_011543063.1:c.430T=	XP_011541365.1:p.Cys144=
XM_011543064.1:c.262T=	XP_011541366.1:p.Cys88=
XM_011543065.1:c.256T=	XP_011541367.1:p.Cys86=
XM_011543066.1:c.430T=	XP_011541368.1:p.Cys144=
NM_001363563.1:c.430T=	NP_001350492.1:p.Cys144=
XM_017018552.2:c.256T=	XP_016874041.1:p.Cys86=
XM_024448767.1:c.169T=	XP_024304535.1:p.Cys57=
XR_001748034.2:n.714T=
NM_001363563.2:c.430T=	NP_001350492.1:p.Cys144=
NM_006028.5:c.463T= MANE Select	NP_006019.1:p.Cys155=