Canonical Allele Identifier: CA2001397959

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932384G= , CM000673.2:g.113932384G=	GRCh38
NC_000011.9:g.113803106G= , CM000673.1:g.113803106G=	GRCh37
NC_000011.8:g.113308316G=	NCBI36
NG_011483.1:g.32518G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.464G= MANE Select	ENSP00000260191.2:p.Cys155=
ENST00000260191.7:c.464G=	ENSP00000260191.2:p.Cys155=
ENST00000260191.6:c.464G=	ENSP00000260191.2:p.Cys155=
ENST00000537778.5:c.431G=	ENSP00000443118.1:p.Cys144=
ENST00000543092.1:c.250G=
NM_006028.4:c.464G=	NP_006019.1:p.Cys155=
XM_011543063.1:c.431G=	XP_011541365.1:p.Cys144=
XM_011543064.1:c.263G=	XP_011541366.1:p.Cys88=
XM_011543065.1:c.257G=	XP_011541367.1:p.Cys86=
XM_011543066.1:c.431G=	XP_011541368.1:p.Cys144=
NM_001363563.1:c.431G=	NP_001350492.1:p.Cys144=
XM_017018552.2:c.257G=	XP_016874041.1:p.Cys86=
XM_024448767.1:c.170G=	XP_024304535.1:p.Cys57=
XR_001748034.2:n.715G=
NM_001363563.2:c.431G=	NP_001350492.1:p.Cys144=
NM_006028.5:c.464G= MANE Select	NP_006019.1:p.Cys155=