Canonical Allele Identifier: CA2001397795

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932059A= , CM000673.2:g.113932059A=	GRCh38
NC_000011.9:g.113802781A= , CM000673.1:g.113802781A=	GRCh37
NC_000011.8:g.113307991A=	NCBI36
NG_011483.1:g.32193A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.368+192A= MANE Select	ENSP00000260191.2:n.368+192A=
ENST00000260191.7:c.368+192A=	ENSP00000260191.2:n.368+192A=
ENST00000260191.6:c.368+192A=	ENSP00000260191.2:n.368+192A=
ENST00000537778.5:c.335+192A=	ENSP00000443118.1:n.335+192A=
ENST00000543092.1:c.154+192A=
NM_006028.4:c.368+192A=	NP_006019.1:n.368+192A=
XM_011543063.1:c.335+192A=	XP_011541365.1:n.335+192A=
XM_011543064.1:c.167+192A=	XP_011541366.1:n.167+192A=
XM_011543065.1:c.161+192A=	XP_011541367.1:n.161+192A=
XM_011543066.1:c.335+192A=	XP_011541368.1:n.335+192A=
NM_001363563.1:c.335+192A=	NP_001350492.1:n.335+192A=
XM_017018552.2:c.161+192A=	XP_016874041.1:n.161+192A=
XM_024448767.1:c.74+192A=	XP_024304535.1:n.74+192A=
XR_001748034.2:n.619+192A=
NM_001363563.2:c.335+192A=	NP_001350492.1:n.335+192A=
NM_006028.5:c.368+192A= MANE Select	NP_006019.1:n.368+192A=