Canonical Allele Identifier: CA2001397930

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932327A= , CM000673.2:g.113932327A=	GRCh38
NC_000011.9:g.113803049A= , CM000673.1:g.113803049A=	GRCh37
NC_000011.8:g.113308259A=	NCBI36
NG_011483.1:g.32461A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.407A= MANE Select	ENSP00000260191.2:p.Tyr136=
ENST00000260191.7:c.407A=	ENSP00000260191.2:p.Tyr136=
ENST00000260191.6:c.407A=	ENSP00000260191.2:p.Tyr136=
ENST00000537778.5:c.374A=	ENSP00000443118.1:p.Tyr125=
ENST00000543092.1:c.193A=
NM_006028.4:c.407A=	NP_006019.1:p.Tyr136=
XM_011543063.1:c.374A=	XP_011541365.1:p.Tyr125=
XM_011543064.1:c.206A=	XP_011541366.1:p.Tyr69=
XM_011543065.1:c.200A=	XP_011541367.1:p.Tyr67=
XM_011543066.1:c.374A=	XP_011541368.1:p.Tyr125=
NM_001363563.1:c.374A=	NP_001350492.1:p.Tyr125=
XM_017018552.2:c.200A=	XP_016874041.1:p.Tyr67=
XM_024448767.1:c.113A=	XP_024304535.1:p.Tyr38=
XR_001748034.2:n.658A=
NM_001363563.2:c.374A=	NP_001350492.1:p.Tyr125=
NM_006028.5:c.407A= MANE Select	NP_006019.1:p.Tyr136=