Canonical Allele Identifier: CA391462150

Gene: GABRB3

Linked Data

• MyVariant Identifiers: chr15:g.26806255A>T (hg19) ; chr15:g.26561108A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561108A>T , CM000677.2:g.26561108A>T	GRCh38
NC_000015.9:g.26806255A>T , CM000677.1:g.26806255A>T	GRCh37
NC_000015.8:g.24357348A>T	NCBI36
NG_012836.1:g.217673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.904T>A	ENSP00000299267.4:p.Tyr302Asn
ENST00000311550.10:c.904T>A MANE Select	ENSP00000308725.5:p.Tyr302Asn
ENST00000635832.1:n.947T>A
ENST00000635994.1:c.587T>A
ENST00000636466.1:c.649T>A	ENSP00000489768.1:p.Tyr217Asn
ENST00000638099.1:c.805T>A	ENSP00000490678.1:p.Tyr269Asn
ENST00000299267.8:c.904T>A	ENSP00000299267.4:p.Tyr302Asn
ENST00000311550.9:c.904T>A	ENSP00000308725.5:p.Tyr302Asn
ENST00000400188.7:c.691T>A	ENSP00000383049.3:p.Tyr231Asn
ENST00000541819.6:c.1072T>A	ENSP00000442408.2:p.Tyr358Asn
ENST00000545868.4:c.649T>A	ENSP00000439169.1:p.Tyr217Asn
ENST00000554556.5:c.*365T>A	ENSP00000451077.1:n.*365T>A
ENST00000555094.5:n.816T>A
ENST00000555632.5:c.*736T>A	ENSP00000452041.1:n.*736T>A
ENST00000622697.4:c.649T>A	ENSP00000481004.1:p.Tyr217Asn
ENST00000628124.2:c.649T>A	ENSP00000486819.1:p.Tyr217Asn
NM_000814.5:c.904T>A	NP_000805.1:p.Tyr302Asn
NM_001191320.1:c.649T>A	NP_001178249.1:p.Tyr217Asn
NM_001191321.2:c.691T>A	NP_001178250.1:p.Tyr231Asn
NM_001278631.1:c.649T>A	NP_001265560.1:p.Tyr217Asn
NM_021912.4:c.904T>A	NP_068712.1:p.Tyr302Asn
XM_011521428.1:c.727T>A	XP_011519730.1:p.Tyr243Asn
XM_011521428.3:c.727T>A	XP_011519730.1:p.Tyr243Asn
NM_000814.6:c.904T>A MANE Select	NP_000805.1:p.Tyr302Asn
NM_001191321.3:c.691T>A	NP_001178250.1:p.Tyr231Asn
NM_021912.5:c.904T>A	NP_068712.1:p.Tyr302Asn
NM_001191320.2:c.649T>A	NP_001178249.1:p.Tyr217Asn
NM_001278631.2:c.649T>A	NP_001265560.1:p.Tyr217Asn