Canonical Allele Identifier: CA2001397913

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932297T= , CM000673.2:g.113932297T=	GRCh38
NC_000011.9:g.113803019T= , CM000673.1:g.113803019T=	GRCh37
NC_000011.8:g.113308229T=	NCBI36
NG_011483.1:g.32431T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.377T= MANE Select	ENSP00000260191.2:p.Ile126=
ENST00000260191.7:c.377T=	ENSP00000260191.2:p.Ile126=
ENST00000260191.6:c.377T=	ENSP00000260191.2:p.Ile126=
ENST00000537778.5:c.344T=	ENSP00000443118.1:p.Ile115=
ENST00000543092.1:c.163T=
NM_006028.4:c.377T=	NP_006019.1:p.Ile126=
XM_011543063.1:c.344T=	XP_011541365.1:p.Ile115=
XM_011543064.1:c.176T=	XP_011541366.1:p.Ile59=
XM_011543065.1:c.170T=	XP_011541367.1:p.Ile57=
XM_011543066.1:c.344T=	XP_011541368.1:p.Ile115=
NM_001363563.1:c.344T=	NP_001350492.1:p.Ile115=
XM_017018552.2:c.170T=	XP_016874041.1:p.Ile57=
XM_024448767.1:c.83T=	XP_024304535.1:p.Ile28=
XR_001748034.2:n.628T=
NM_001363563.2:c.344T=	NP_001350492.1:p.Ile115=
NM_006028.5:c.377T= MANE Select	NP_006019.1:p.Ile126=