Canonical Allele Identifier: CA2001382934

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910312T= , CM000673.2:g.113910312T=	GRCh38
NC_000011.9:g.113781034T= , CM000673.1:g.113781034T=	GRCh37
NC_000011.8:g.113286244T=	NCBI36
NG_011483.1:g.10446T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.213+857T= MANE Select	ENSP00000260191.2:n.213+857T=
ENST00000260191.7:c.213+857T=	ENSP00000260191.2:n.213+857T=
ENST00000260191.6:c.213+857T=	ENSP00000260191.2:n.213+857T=
ENST00000537778.5:c.180+857T=	ENSP00000443118.1:n.180+857T=
NM_006028.4:c.213+857T=	NP_006019.1:n.213+857T=
XM_011543063.1:c.180+857T=	XP_011541365.1:n.180+857T=
XM_011543064.1:c.12+11229T=	XP_011541366.1:n.12+11229T=
XM_011543066.1:c.180+857T=	XP_011541368.1:n.180+857T=
NM_001363563.1:c.180+857T=	NP_001350492.1:n.180+857T=
XM_024448767.1:c.-82+857T=	XP_024304535.1:n.-82+857T=
XR_001748034.2:n.464+857T=
NM_001363563.2:c.180+857T=	NP_001350492.1:n.180+857T=
NM_006028.5:c.213+857T= MANE Select	NP_006019.1:n.213+857T=