Canonical Allele Identifier: CA2165760515
Gene: GABRB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.26580364T= , CM000677.2:g.26580364T= GRCh38
NC_000015.9:g.26825511T= , CM000677.1:g.26825511T= GRCh37
NC_000015.8:g.24376604T= NCBI36
NG_012836.1:g.198417A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299267.9:c.637A= ENSP00000299267.4:p.Ile213=
ENST00000311550.10:c.637A= MANE Select ENSP00000308725.5:p.Ile213=
ENST00000635832.1:n.680A=
ENST00000635994.1:c.320A=
ENST00000636466.1:c.382A= ENSP00000489768.1:p.Ile128=
ENST00000638099.1:c.538A= ENSP00000490678.1:p.Ile180=
ENST00000299267.8:c.637A= ENSP00000299267.4:p.Ile213=
ENST00000311550.9:c.637A= ENSP00000308725.5:p.Ile213=
ENST00000400188.7:c.424A= ENSP00000383049.3:p.Ile142=
ENST00000541819.6:c.805A= ENSP00000442408.2:p.Ile269=
ENST00000545868.4:c.382A= ENSP00000439169.1:p.Ile128=
ENST00000554556.5:c.*98A= ENSP00000451077.1:n.*98A=
ENST00000555094.5:n.549A=
ENST00000555632.5:c.*469A= ENSP00000452041.1:n.*469A=
ENST00000557765.1:n.308A=
ENST00000622697.4:c.382A= ENSP00000481004.1:p.Ile128=
ENST00000628124.2:c.382A= ENSP00000486819.1:p.Ile128=
NM_000814.5:c.637A= NP_000805.1:p.Ile213=
NM_001191320.1:c.382A= NP_001178249.1:p.Ile128=
NM_001191321.2:c.424A= NP_001178250.1:p.Ile142=
NM_001278631.1:c.382A= NP_001265560.1:p.Ile128=
NM_021912.4:c.637A= NP_068712.1:p.Ile213=
XM_011521428.1:c.460A= XP_011519730.1:p.Ile154=
XM_011521428.3:c.460A= XP_011519730.1:p.Ile154=
NM_000814.6:c.637A= MANE Select NP_000805.1:p.Ile213=
NM_001191321.3:c.424A= NP_001178250.1:p.Ile142=
NM_021912.5:c.637A= NP_068712.1:p.Ile213=
NM_001191320.2:c.382A= NP_001178249.1:p.Ile128=
NM_001278631.2:c.382A= NP_001265560.1:p.Ile128=