Canonical Allele Identifier: CA362172258

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160838046G>A (hg19) ; chr5:g.161411040G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161411040G>A , CM000667.2:g.161411040G>A	GRCh38
NC_000005.9:g.160838046G>A , CM000667.1:g.160838046G>A	GRCh37
NC_000005.8:g.160770624G>A	NCBI36
NG_047050.1:g.142085C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.476C>T	ENSP00000274547.2:p.Ala159Val
ENST00000393959.6:c.476C>T MANE Select	ENSP00000377531.1:p.Ala159Val
ENST00000674514.1:n.558C>T
ENST00000675081.1:c.224C>T	ENSP00000502207.1:p.Ala75Val
ENST00000675303.1:c.476C>T	ENSP00000502748.1:p.Ala159Val
ENST00000675381.1:c.224C>T	ENSP00000501968.1:p.Ala75Val
ENST00000675773.1:c.476C>T	ENSP00000502701.1:p.Ala159Val
ENST00000274547.6:c.476C>T	ENSP00000274547.2:p.Ala159Val
ENST00000353437.10:c.476C>T	ENSP00000274546.6:p.Ala159Val
ENST00000393959.5:c.476C>T	ENSP00000377531.1:p.Ala159Val
ENST00000517547.5:c.-5C>T	ENSP00000429750.1:n.-5C>T
ENST00000517901.5:c.287C>T	ENSP00000430532.1:p.Ala96Val
ENST00000520240.5:c.476C>T	ENSP00000429320.1:p.Ala159Val
ENST00000612710.1:c.287C>T	ENSP00000480066.1:p.Ala96Val
NM_000813.2:c.476C>T	NP_000804.1:p.Ala159Val
NM_021911.2:c.476C>T	NP_068711.1:p.Ala159Val
NM_000813.3:c.476C>T	NP_000804.1:p.Ala159Val
NM_001371727.1:c.476C>T MANE Select	NP_001358656.1:p.Ala159Val
NM_021911.3:c.476C>T	NP_068711.1:p.Ala159Val