Canonical Allele Identifier: CA2001382926

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910287G= , CM000673.2:g.113910287G=	GRCh38
NC_000011.9:g.113781009G= , CM000673.1:g.113781009G=	GRCh37
NC_000011.8:g.113286219G=	NCBI36
NG_011483.1:g.10421G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+832G= MANE Select	ENSP00000260191.2:n.213+832G=
ENST00000260191.7:c.213+832G=	ENSP00000260191.2:n.213+832G=
ENST00000260191.6:c.213+832G=	ENSP00000260191.2:n.213+832G=
ENST00000537778.5:c.180+832G=	ENSP00000443118.1:n.180+832G=
NM_006028.4:c.213+832G=	NP_006019.1:n.213+832G=
XM_011543063.1:c.180+832G=	XP_011541365.1:n.180+832G=
XM_011543064.1:c.12+11204G=	XP_011541366.1:n.12+11204G=
XM_011543066.1:c.180+832G=	XP_011541368.1:n.180+832G=
NM_001363563.1:c.180+832G=	NP_001350492.1:n.180+832G=
XM_024448767.1:c.-82+832G=	XP_024304535.1:n.-82+832G=
XR_001748034.2:n.464+832G=
NM_001363563.2:c.180+832G=	NP_001350492.1:n.180+832G=
NM_006028.5:c.213+832G= MANE Select	NP_006019.1:n.213+832G=