Canonical Allele Identifier: CA391463964

Gene: GABRB3

Linked Data

• MyVariant Identifiers: chr15:g.26825504T>A (hg19) ; chr15:g.26580357T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26580357T>A , CM000677.2:g.26580357T>A	GRCh38
NC_000015.9:g.26825504T>A , CM000677.1:g.26825504T>A	GRCh37
NC_000015.8:g.24376597T>A	NCBI36
NG_012836.1:g.198424A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299267.9:c.644A>T	ENSP00000299267.4:p.Glu215Val
ENST00000311550.10:c.644A>T MANE Select	ENSP00000308725.5:p.Glu215Val
ENST00000635832.1:n.687A>T
ENST00000635994.1:c.327A>T
ENST00000636466.1:c.389A>T	ENSP00000489768.1:p.Glu130Val
ENST00000638099.1:c.545A>T	ENSP00000490678.1:p.Glu182Val
ENST00000299267.8:c.644A>T	ENSP00000299267.4:p.Glu215Val
ENST00000311550.9:c.644A>T	ENSP00000308725.5:p.Glu215Val
ENST00000400188.7:c.431A>T	ENSP00000383049.3:p.Glu144Val
ENST00000541819.6:c.812A>T	ENSP00000442408.2:p.Glu271Val
ENST00000545868.4:c.389A>T	ENSP00000439169.1:p.Glu130Val
ENST00000554556.5:c.*105A>T	ENSP00000451077.1:n.*105A>T
ENST00000555094.5:n.556A>T
ENST00000555632.5:c.*476A>T	ENSP00000452041.1:n.*476A>T
ENST00000557765.1:n.315A>T
ENST00000622697.4:c.389A>T	ENSP00000481004.1:p.Glu130Val
ENST00000628124.2:c.389A>T	ENSP00000486819.1:p.Glu130Val
NM_000814.5:c.644A>T	NP_000805.1:p.Glu215Val
NM_001191320.1:c.389A>T	NP_001178249.1:p.Glu130Val
NM_001191321.2:c.431A>T	NP_001178250.1:p.Glu144Val
NM_001278631.1:c.389A>T	NP_001265560.1:p.Glu130Val
NM_021912.4:c.644A>T	NP_068712.1:p.Glu215Val
XM_011521428.1:c.467A>T	XP_011519730.1:p.Glu156Val
XM_011521428.3:c.467A>T	XP_011519730.1:p.Glu156Val
NM_000814.6:c.644A>T MANE Select	NP_000805.1:p.Glu215Val
NM_001191321.3:c.431A>T	NP_001178250.1:p.Glu144Val
NM_021912.5:c.644A>T	NP_068712.1:p.Glu215Val
NM_001191320.2:c.389A>T	NP_001178249.1:p.Glu130Val
NM_001278631.2:c.389A>T	NP_001265560.1:p.Glu130Val