Canonical Allele Identifier: CA2165747225

Gene: GABRB3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561157T= , CM000677.2:g.26561157T=	GRCh38
NC_000015.9:g.26806304T= , CM000677.1:g.26806304T=	GRCh37
NC_000015.8:g.24357397T=	NCBI36
NG_012836.1:g.217624A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.855A=	ENSP00000299267.4:p.Thr285=
ENST00000311550.10:c.855A= MANE Select	ENSP00000308725.5:p.Thr285=
ENST00000635832.1:n.898A=
ENST00000635994.1:c.538A=
ENST00000636466.1:c.600A=	ENSP00000489768.1:p.Thr200=
ENST00000638099.1:c.756A=	ENSP00000490678.1:p.Thr252=
ENST00000299267.8:c.855A=	ENSP00000299267.4:p.Thr285=
ENST00000311550.9:c.855A=	ENSP00000308725.5:p.Thr285=
ENST00000400188.7:c.642A=	ENSP00000383049.3:p.Thr214=
ENST00000541819.6:c.1023A=	ENSP00000442408.2:p.Thr341=
ENST00000545868.4:c.600A=	ENSP00000439169.1:p.Thr200=
ENST00000554556.5:c.*316A=	ENSP00000451077.1:n.*316A=
ENST00000555094.5:n.767A=
ENST00000555632.5:c.*687A=	ENSP00000452041.1:n.*687A=
ENST00000557765.1:n.526A=
ENST00000622697.4:c.600A=	ENSP00000481004.1:p.Thr200=
ENST00000628124.2:c.600A=	ENSP00000486819.1:p.Thr200=
NM_000814.5:c.855A=	NP_000805.1:p.Thr285=
NM_001191320.1:c.600A=	NP_001178249.1:p.Thr200=
NM_001191321.2:c.642A=	NP_001178250.1:p.Thr214=
NM_001278631.1:c.600A=	NP_001265560.1:p.Thr200=
NM_021912.4:c.855A=	NP_068712.1:p.Thr285=
XM_011521428.1:c.678A=	XP_011519730.1:p.Thr226=
XM_011521428.3:c.678A=	XP_011519730.1:p.Thr226=
NM_000814.6:c.855A= MANE Select	NP_000805.1:p.Thr285=
NM_001191321.3:c.642A=	NP_001178250.1:p.Thr214=
NM_021912.5:c.855A=	NP_068712.1:p.Thr285=
NM_001191320.2:c.600A=	NP_001178249.1:p.Thr200=
NM_001278631.2:c.600A=	NP_001265560.1:p.Thr200=