Canonical Allele Identifier: CA2001382923

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910281C= , CM000673.2:g.113910281C=	GRCh38
NC_000011.9:g.113781003C= , CM000673.1:g.113781003C=	GRCh37
NC_000011.8:g.113286213C=	NCBI36
NG_011483.1:g.10415C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+826C= MANE Select	ENSP00000260191.2:n.213+826C=
ENST00000260191.7:c.213+826C=	ENSP00000260191.2:n.213+826C=
ENST00000260191.6:c.213+826C=	ENSP00000260191.2:n.213+826C=
ENST00000537778.5:c.180+826C=	ENSP00000443118.1:n.180+826C=
NM_006028.4:c.213+826C=	NP_006019.1:n.213+826C=
XM_011543063.1:c.180+826C=	XP_011541365.1:n.180+826C=
XM_011543064.1:c.12+11198C=	XP_011541366.1:n.12+11198C=
XM_011543066.1:c.180+826C=	XP_011541368.1:n.180+826C=
NM_001363563.1:c.180+826C=	NP_001350492.1:n.180+826C=
XM_024448767.1:c.-82+826C=	XP_024304535.1:n.-82+826C=
XR_001748034.2:n.464+826C=
NM_001363563.2:c.180+826C=	NP_001350492.1:n.180+826C=
NM_006028.5:c.213+826C= MANE Select	NP_006019.1:n.213+826C=