Canonical Allele Identifier: CA362175252

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160758012C>T (hg19) ; chr5:g.161331005C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161331005C>T , CM000667.2:g.161331005C>T	GRCh38
NC_000005.9:g.160758012C>T , CM000667.1:g.160758012C>T	GRCh37
NC_000005.8:g.160690590C>T	NCBI36
NG_047050.1:g.222120G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000274547.7:c.955G>A	ENSP00000274547.2:p.Ala319Thr
ENST00000393959.6:c.955G>A MANE Select	ENSP00000377531.1:p.Ala319Thr
ENST00000674514.1:n.1037G>A
ENST00000675081.1:c.*414G>A	ENSP00000502207.1:n.*414G>A
ENST00000675303.1:c.955G>A	ENSP00000502748.1:p.Ala319Thr
ENST00000675381.1:c.703G>A	ENSP00000501968.1:p.Ala235Thr
ENST00000675746.1:c.205G>A	ENSP00000502391.1:p.Ala69Thr
ENST00000675773.1:c.955G>A	ENSP00000502701.1:p.Ala319Thr
ENST00000274547.6:c.955G>A	ENSP00000274547.2:p.Ala319Thr
ENST00000353437.10:c.955G>A	ENSP00000274546.6:p.Ala319Thr
ENST00000393959.5:c.955G>A	ENSP00000377531.1:p.Ala319Thr
ENST00000517547.5:c.475G>A	ENSP00000429750.1:p.Ala159Thr
ENST00000517901.5:c.766G>A	ENSP00000430532.1:p.Ala256Thr
ENST00000520240.5:c.955G>A	ENSP00000429320.1:p.Ala319Thr
ENST00000612710.1:c.766G>A	ENSP00000480066.1:p.Ala256Thr
NM_000813.2:c.955G>A	NP_000804.1:p.Ala319Thr
NM_021911.2:c.955G>A	NP_068711.1:p.Ala319Thr
XM_011534501.1:c.205G>A	XP_011532803.1:p.Ala69Thr
NM_000813.3:c.955G>A	NP_000804.1:p.Ala319Thr
NM_001371727.1:c.955G>A MANE Select	NP_001358656.1:p.Ala319Thr
NM_021911.3:c.955G>A	NP_068711.1:p.Ala319Thr