Canonical Allele Identifier: CA1596016619

Gene: GABRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161410945C= , CM000667.2:g.161410945C=	GRCh38
NC_000005.9:g.160837951C= , CM000667.1:g.160837951C=	GRCh37
NC_000005.8:g.160770529C=	NCBI36
NG_047050.1:g.142180G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.541+30G=	ENSP00000274547.2:n.541+30G=
ENST00000393959.6:c.541+30G= MANE Select	ENSP00000377531.1:n.541+30G=
ENST00000674514.1:n.623+30G=
ENST00000675081.1:c.289+30G=	ENSP00000502207.1:n.289+30G=
ENST00000675303.1:c.541+30G=	ENSP00000502748.1:n.541+30G=
ENST00000675381.1:c.289+30G=	ENSP00000501968.1:n.289+30G=
ENST00000675773.1:c.541+30G=	ENSP00000502701.1:n.541+30G=
ENST00000274547.6:c.541+30G=	ENSP00000274547.2:n.541+30G=
ENST00000353437.10:c.541+30G=	ENSP00000274546.6:n.541+30G=
ENST00000393959.5:c.541+30G=	ENSP00000377531.1:n.541+30G=
ENST00000517547.5:c.61+30G=	ENSP00000429750.1:n.61+30G=
ENST00000517901.5:c.352+30G=	ENSP00000430532.1:n.352+30G=
ENST00000520240.5:c.541+30G=	ENSP00000429320.1:n.541+30G=
ENST00000612710.1:c.352+30G=	ENSP00000480066.1:n.352+30G=
NM_000813.2:c.541+30G=	NP_000804.1:n.541+30G=
NM_021911.2:c.541+30G=	NP_068711.1:n.541+30G=
NM_000813.3:c.541+30G=	NP_000804.1:n.541+30G=
NM_001371727.1:c.541+30G= MANE Select	NP_001358656.1:n.541+30G=
NM_021911.3:c.541+30G=	NP_068711.1:n.541+30G=