Canonical Allele Identifier: CA2001397960

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932386A= , CM000673.2:g.113932386A=	GRCh38
NC_000011.9:g.113803108A= , CM000673.1:g.113803108A=	GRCh37
NC_000011.8:g.113308318A=	NCBI36
NG_011483.1:g.32520A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.466A= MANE Select	ENSP00000260191.2:p.Ser156=
ENST00000260191.7:c.466A=	ENSP00000260191.2:p.Ser156=
ENST00000260191.6:c.466A=	ENSP00000260191.2:p.Ser156=
ENST00000537778.5:c.433A=	ENSP00000443118.1:p.Ser145=
ENST00000543092.1:c.252A=
NM_006028.4:c.466A=	NP_006019.1:p.Ser156=
XM_011543063.1:c.433A=	XP_011541365.1:p.Ser145=
XM_011543064.1:c.265A=	XP_011541366.1:p.Ser89=
XM_011543065.1:c.259A=	XP_011541367.1:p.Ser87=
XM_011543066.1:c.433A=	XP_011541368.1:p.Ser145=
NM_001363563.1:c.433A=	NP_001350492.1:p.Ser145=
XM_017018552.2:c.259A=	XP_016874041.1:p.Ser87=
XM_024448767.1:c.172A=	XP_024304535.1:p.Ser58=
XR_001748034.2:n.717A=
NM_001363563.2:c.433A=	NP_001350492.1:p.Ser145=
NM_006028.5:c.466A= MANE Select	NP_006019.1:p.Ser156=