Canonical Allele Identifier: CA489238783

Gene: GABRB3

Linked Data

• MyVariant Identifiers: chr15:g.26806286G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561139G>C , CM000677.2:g.26561139G>C	GRCh38
NC_000015.9:g.26806286G>C , CM000677.1:g.26806286G>C	GRCh37
NC_000015.8:g.24357379G>C	NCBI36
NG_012836.1:g.217642C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.873C>G	ENSP00000299267.4:p.Thr291=
ENST00000311550.10:c.873C>G MANE Select	ENSP00000308725.5:p.Thr291=
ENST00000635832.1:n.916C>G
ENST00000635994.1:c.556C>G
ENST00000636466.1:c.618C>G	ENSP00000489768.1:p.Thr206=
ENST00000638099.1:c.774C>G	ENSP00000490678.1:p.Thr258=
ENST00000299267.8:c.873C>G	ENSP00000299267.4:p.Thr291=
ENST00000311550.9:c.873C>G	ENSP00000308725.5:p.Thr291=
ENST00000400188.7:c.660C>G	ENSP00000383049.3:p.Thr220=
ENST00000541819.6:c.1041C>G	ENSP00000442408.2:p.Thr347=
ENST00000545868.4:c.618C>G	ENSP00000439169.1:p.Thr206=
ENST00000554556.5:c.*334C>G	ENSP00000451077.1:n.*334C>G
ENST00000555094.5:n.785C>G
ENST00000555632.5:c.*705C>G	ENSP00000452041.1:n.*705C>G
ENST00000557765.1:n.544C>G
ENST00000622697.4:c.618C>G	ENSP00000481004.1:p.Thr206=
ENST00000628124.2:c.618C>G	ENSP00000486819.1:p.Thr206=
NM_000814.5:c.873C>G	NP_000805.1:p.Thr291=
NM_001191320.1:c.618C>G	NP_001178249.1:p.Thr206=
NM_001191321.2:c.660C>G	NP_001178250.1:p.Thr220=
NM_001278631.1:c.618C>G	NP_001265560.1:p.Thr206=
NM_021912.4:c.873C>G	NP_068712.1:p.Thr291=
XM_011521428.1:c.696C>G	XP_011519730.1:p.Thr232=
XM_011521428.3:c.696C>G	XP_011519730.1:p.Thr232=
NM_000814.6:c.873C>G MANE Select	NP_000805.1:p.Thr291=
NM_001191321.3:c.660C>G	NP_001178250.1:p.Thr220=
NM_021912.5:c.873C>G	NP_068712.1:p.Thr291=
NM_001191320.2:c.618C>G	NP_001178249.1:p.Thr206=
NM_001278631.2:c.618C>G	NP_001265560.1:p.Thr206=