Canonical Allele Identifier: CA2001397992

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932456C= , CM000673.2:g.113932456C=	GRCh38
NC_000011.9:g.113803178C= , CM000673.1:g.113803178C=	GRCh37
NC_000011.8:g.113308388C=	NCBI36
NG_011483.1:g.32590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.536C= MANE Select	ENSP00000260191.2:p.Thr179=
ENST00000260191.7:c.536C=	ENSP00000260191.2:p.Thr179=
ENST00000260191.6:c.536C=	ENSP00000260191.2:p.Thr179=
ENST00000537778.5:c.503C=	ENSP00000443118.1:p.Thr168=
ENST00000543092.1:c.322C=
NM_006028.4:c.536C=	NP_006019.1:p.Thr179=
XM_011543063.1:c.503C=	XP_011541365.1:p.Thr168=
XM_011543064.1:c.335C=	XP_011541366.1:p.Thr112=
XM_011543065.1:c.329C=	XP_011541367.1:p.Thr110=
XM_011543066.1:c.503C=	XP_011541368.1:p.Thr168=
NM_001363563.1:c.503C=	NP_001350492.1:p.Thr168=
XM_017018552.2:c.329C=	XP_016874041.1:p.Thr110=
XM_024448767.1:c.242C=	XP_024304535.1:p.Thr81=
XR_001748034.2:n.787C=
NM_001363563.2:c.503C=	NP_001350492.1:p.Thr168=
NM_006028.5:c.536C= MANE Select	NP_006019.1:p.Thr179=