Canonical Allele Identifier: CA2165747245

Gene: GABRB3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561171T= , CM000677.2:g.26561171T=	GRCh38
NC_000015.9:g.26806318T= , CM000677.1:g.26806318T=	GRCh37
NC_000015.8:g.24357411T=	NCBI36
NG_012836.1:g.217610A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.841A=	ENSP00000299267.4:p.Thr281=
ENST00000311550.10:c.841A= MANE Select	ENSP00000308725.5:p.Thr281=
ENST00000635832.1:n.884A=
ENST00000635994.1:c.524A=
ENST00000636466.1:c.586A=	ENSP00000489768.1:p.Thr196=
ENST00000638099.1:c.742A=	ENSP00000490678.1:p.Thr248=
ENST00000299267.8:c.841A=	ENSP00000299267.4:p.Thr281=
ENST00000311550.9:c.841A=	ENSP00000308725.5:p.Thr281=
ENST00000400188.7:c.628A=	ENSP00000383049.3:p.Thr210=
ENST00000541819.6:c.1009A=	ENSP00000442408.2:p.Thr337=
ENST00000545868.4:c.586A=	ENSP00000439169.1:p.Thr196=
ENST00000554556.5:c.*302A=	ENSP00000451077.1:n.*302A=
ENST00000555094.5:n.753A=
ENST00000555632.5:c.*673A=	ENSP00000452041.1:n.*673A=
ENST00000557765.1:n.512A=
ENST00000622697.4:c.586A=	ENSP00000481004.1:p.Thr196=
ENST00000628124.2:c.586A=	ENSP00000486819.1:p.Thr196=
NM_000814.5:c.841A=	NP_000805.1:p.Thr281=
NM_001191320.1:c.586A=	NP_001178249.1:p.Thr196=
NM_001191321.2:c.628A=	NP_001178250.1:p.Thr210=
NM_001278631.1:c.586A=	NP_001265560.1:p.Thr196=
NM_021912.4:c.841A=	NP_068712.1:p.Thr281=
XM_011521428.1:c.664A=	XP_011519730.1:p.Thr222=
XM_011521428.3:c.664A=	XP_011519730.1:p.Thr222=
NM_000814.6:c.841A= MANE Select	NP_000805.1:p.Thr281=
NM_001191321.3:c.628A=	NP_001178250.1:p.Thr210=
NM_021912.5:c.841A=	NP_068712.1:p.Thr281=
NM_001191320.2:c.586A=	NP_001178249.1:p.Thr196=
NM_001278631.2:c.586A=	NP_001265560.1:p.Thr196=