Canonical Allele Identifier: CA2001397922

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932314C= , CM000673.2:g.113932314C=	GRCh38
NC_000011.9:g.113803036C= , CM000673.1:g.113803036C=	GRCh37
NC_000011.8:g.113308246C=	NCBI36
NG_011483.1:g.32448C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.394C= MANE Select	ENSP00000260191.2:p.Leu132=
ENST00000260191.7:c.394C=	ENSP00000260191.2:p.Leu132=
ENST00000260191.6:c.394C=	ENSP00000260191.2:p.Leu132=
ENST00000537778.5:c.361C=	ENSP00000443118.1:p.Leu121=
ENST00000543092.1:c.180C=
NM_006028.4:c.394C=	NP_006019.1:p.Leu132=
XM_011543063.1:c.361C=	XP_011541365.1:p.Leu121=
XM_011543064.1:c.193C=	XP_011541366.1:p.Leu65=
XM_011543065.1:c.187C=	XP_011541367.1:p.Leu63=
XM_011543066.1:c.361C=	XP_011541368.1:p.Leu121=
NM_001363563.1:c.361C=	NP_001350492.1:p.Leu121=
XM_017018552.2:c.187C=	XP_016874041.1:p.Leu63=
XM_024448767.1:c.100C=	XP_024304535.1:p.Leu34=
XR_001748034.2:n.645C=
NM_001363563.2:c.361C=	NP_001350492.1:p.Leu121=
NM_006028.5:c.394C= MANE Select	NP_006019.1:p.Leu132=