Canonical Allele Identifier: CA447605085

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160838018T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161411012T>G , CM000667.2:g.161411012T>G	GRCh38
NC_000005.9:g.160838018T>G , CM000667.1:g.160838018T>G	GRCh37
NC_000005.8:g.160770596T>G	NCBI36
NG_047050.1:g.142113A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.504A>C	ENSP00000274547.2:p.Pro168=
ENST00000393959.6:c.504A>C MANE Select	ENSP00000377531.1:p.Pro168=
ENST00000674514.1:n.586A>C
ENST00000675081.1:c.252A>C	ENSP00000502207.1:p.Pro84=
ENST00000675303.1:c.504A>C	ENSP00000502748.1:p.Pro168=
ENST00000675381.1:c.252A>C	ENSP00000501968.1:p.Pro84=
ENST00000675773.1:c.504A>C	ENSP00000502701.1:p.Pro168=
ENST00000274547.6:c.504A>C	ENSP00000274547.2:p.Pro168=
ENST00000353437.10:c.504A>C	ENSP00000274546.6:p.Pro168=
ENST00000393959.5:c.504A>C	ENSP00000377531.1:p.Pro168=
ENST00000517547.5:c.24A>C	ENSP00000429750.1:p.Pro8=
ENST00000517901.5:c.315A>C	ENSP00000430532.1:p.Pro105=
ENST00000520240.5:c.504A>C	ENSP00000429320.1:p.Pro168=
ENST00000612710.1:c.315A>C	ENSP00000480066.1:p.Pro105=
NM_000813.2:c.504A>C	NP_000804.1:p.Pro168=
NM_021911.2:c.504A>C	NP_068711.1:p.Pro168=
NM_000813.3:c.504A>C	NP_000804.1:p.Pro168=
NM_001371727.1:c.504A>C MANE Select	NP_001358656.1:p.Pro168=
NM_021911.3:c.504A>C	NP_068711.1:p.Pro168=