Canonical Allele Identifier: CA1645371256

Gene: GABRR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.89257779G= , CM000668.2:g.89257779G=	GRCh38
NC_000006.11:g.89967498G= , CM000668.1:g.89967498G=	GRCh37
NC_000006.10:g.90024217G=	NCBI36
NG_033977.1:g.62521C=
NG_033977.2:g.62521C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002043.5:c.1289C= MANE Select	NP_002034.3:p.Thr430=
ENST00000402938.4:c.1289C= MANE Select	ENSP00000386029.4:p.Thr430=
NM_002043.3:c.1289C=	NP_002034.3:p.Thr430=
NM_002043.4:c.1289C=	NP_002034.3:p.Thr430=
ENST00000402938.3:c.1289C=	ENSP00000386029.4:p.Thr430=
ENST00000602432.1:n.1120C=
XM_011535713.1:c.1157C=	XP_011534015.1:p.Thr386=
XM_011535713.2:c.1157C=	XP_011534015.1:p.Thr386=
XM_011535714.1:c.992C=	XP_011534016.1:p.Thr331=
XM_011535714.3:c.992C=	XP_011534016.1:p.Thr331=
XM_011535715.1:c.992C=	XP_011534017.1:p.Thr331=
XM_011535715.3:c.992C=	XP_011534017.1:p.Thr331=
XM_011535716.1:c.992C=	XP_011534018.1:p.Thr331=
XM_011535716.3:c.992C=	XP_011534018.1:p.Thr331=
XM_011535717.1:c.992C=	XP_011534019.1:p.Thr331=
XM_011535717.3:c.992C=	XP_011534019.1:p.Thr331=
XM_011535718.1:c.992C=	XP_011534020.1:p.Thr331=