Canonical Allele Identifier: CA362172229
Gene: GABRB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161411029C>A , CM000667.2:g.161411029C>A GRCh38
NC_000005.9:g.160838035C>A , CM000667.1:g.160838035C>A GRCh37
NC_000005.8:g.160770613C>A NCBI36
NG_047050.1:g.142096G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274547.7:c.487G>T ENSP00000274547.2:p.Asp163Tyr
ENST00000393959.6:c.487G>T MANE Select ENSP00000377531.1:p.Asp163Tyr
ENST00000674514.1:n.569G>T
ENST00000675081.1:c.235G>T ENSP00000502207.1:p.Asp79Tyr
ENST00000675303.1:c.487G>T ENSP00000502748.1:p.Asp163Tyr
ENST00000675381.1:c.235G>T ENSP00000501968.1:p.Asp79Tyr
ENST00000675773.1:c.487G>T ENSP00000502701.1:p.Asp163Tyr
ENST00000274547.6:c.487G>T ENSP00000274547.2:p.Asp163Tyr
ENST00000353437.10:c.487G>T ENSP00000274546.6:p.Asp163Tyr
ENST00000393959.5:c.487G>T ENSP00000377531.1:p.Asp163Tyr
ENST00000517547.5:c.7G>T ENSP00000429750.1:p.Asp3Tyr
ENST00000517901.5:c.298G>T ENSP00000430532.1:p.Asp100Tyr
ENST00000520240.5:c.487G>T ENSP00000429320.1:p.Asp163Tyr
ENST00000612710.1:c.298G>T ENSP00000480066.1:p.Asp100Tyr
NM_000813.2:c.487G>T NP_000804.1:p.Asp163Tyr
NM_021911.2:c.487G>T NP_068711.1:p.Asp163Tyr
NM_000813.3:c.487G>T NP_000804.1:p.Asp163Tyr
NM_001371727.1:c.487G>T MANE Select NP_001358656.1:p.Asp163Tyr
NM_021911.3:c.487G>T NP_068711.1:p.Asp163Tyr