Canonical Allele Identifier: CA2165747284
Gene: GABRB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.26561186A= , CM000677.2:g.26561186A= GRCh38
NC_000015.9:g.26806333A= , CM000677.1:g.26806333A= GRCh37
NC_000015.8:g.24357426A= NCBI36
NG_012836.1:g.217595T=

Transcript Alleles

HGVS Amino-acid change
ENST00000299267.9:c.836-10T= ENSP00000299267.4:n.836-10T=
ENST00000311550.10:c.836-10T= MANE Select ENSP00000308725.5:n.836-10T=
ENST00000635832.1:n.879-10T=
ENST00000635994.1:c.519-10T=
ENST00000636466.1:c.581-10T= ENSP00000489768.1:n.581-10T=
ENST00000638099.1:c.737-10T= ENSP00000490678.1:n.737-10T=
ENST00000299267.8:c.836-10T= ENSP00000299267.4:n.836-10T=
ENST00000311550.9:c.836-10T= ENSP00000308725.5:n.836-10T=
ENST00000400188.7:c.623-10T= ENSP00000383049.3:n.623-10T=
ENST00000541819.6:c.1004-10T= ENSP00000442408.2:n.1004-10T=
ENST00000545868.4:c.581-10T= ENSP00000439169.1:n.581-10T=
ENST00000554556.5:c.*297-10T= ENSP00000451077.1:n.*297-10T=
ENST00000555094.5:n.748-10T=
ENST00000555632.5:c.*668-10T= ENSP00000452041.1:n.*668-10T=
ENST00000557765.1:n.507-10T=
ENST00000622697.4:c.581-10T= ENSP00000481004.1:n.581-10T=
ENST00000628124.2:c.581-10T= ENSP00000486819.1:n.581-10T=
NM_000814.5:c.836-10T= NP_000805.1:n.836-10T=
NM_001191320.1:c.581-10T= NP_001178249.1:n.581-10T=
NM_001191321.2:c.623-10T= NP_001178250.1:n.623-10T=
NM_001278631.1:c.581-10T= NP_001265560.1:n.581-10T=
NM_021912.4:c.836-10T= NP_068712.1:n.836-10T=
XM_011521428.1:c.659-10T= XP_011519730.1:n.659-10T=
XM_011521428.3:c.659-10T= XP_011519730.1:n.659-10T=
NM_000814.6:c.836-10T= MANE Select NP_000805.1:n.836-10T=
NM_001191321.3:c.623-10T= NP_001178250.1:n.623-10T=
NM_021912.5:c.836-10T= NP_068712.1:n.836-10T=
NM_001191320.2:c.581-10T= NP_001178249.1:n.581-10T=
NM_001278631.2:c.581-10T= NP_001265560.1:n.581-10T=