Canonical Allele Identifier: CA391462324

Gene: GABRB3

Linked Data

• MyVariant Identifiers: chr15:g.26806296G>T (hg19) ; chr15:g.26561149G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561149G>T , CM000677.2:g.26561149G>T	GRCh38
NC_000015.9:g.26806296G>T , CM000677.1:g.26806296G>T	GRCh37
NC_000015.8:g.24357389G>T	NCBI36
NG_012836.1:g.217632C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.863C>A	ENSP00000299267.4:p.Thr288Asn
ENST00000311550.10:c.863C>A MANE Select	ENSP00000308725.5:p.Thr288Asn
ENST00000635832.1:n.906C>A
ENST00000635994.1:c.546C>A
ENST00000636466.1:c.608C>A	ENSP00000489768.1:p.Thr203Asn
ENST00000638099.1:c.764C>A	ENSP00000490678.1:p.Thr255Asn
ENST00000299267.8:c.863C>A	ENSP00000299267.4:p.Thr288Asn
ENST00000311550.9:c.863C>A	ENSP00000308725.5:p.Thr288Asn
ENST00000400188.7:c.650C>A	ENSP00000383049.3:p.Thr217Asn
ENST00000541819.6:c.1031C>A	ENSP00000442408.2:p.Thr344Asn
ENST00000545868.4:c.608C>A	ENSP00000439169.1:p.Thr203Asn
ENST00000554556.5:c.*324C>A	ENSP00000451077.1:n.*324C>A
ENST00000555094.5:n.775C>A
ENST00000555632.5:c.*695C>A	ENSP00000452041.1:n.*695C>A
ENST00000557765.1:n.534C>A
ENST00000622697.4:c.608C>A	ENSP00000481004.1:p.Thr203Asn
ENST00000628124.2:c.608C>A	ENSP00000486819.1:p.Thr203Asn
NM_000814.5:c.863C>A	NP_000805.1:p.Thr288Asn
NM_001191320.1:c.608C>A	NP_001178249.1:p.Thr203Asn
NM_001191321.2:c.650C>A	NP_001178250.1:p.Thr217Asn
NM_001278631.1:c.608C>A	NP_001265560.1:p.Thr203Asn
NM_021912.4:c.863C>A	NP_068712.1:p.Thr288Asn
XM_011521428.1:c.686C>A	XP_011519730.1:p.Thr229Asn
XM_011521428.3:c.686C>A	XP_011519730.1:p.Thr229Asn
NM_000814.6:c.863C>A MANE Select	NP_000805.1:p.Thr288Asn
NM_001191321.3:c.650C>A	NP_001178250.1:p.Thr217Asn
NM_021912.5:c.863C>A	NP_068712.1:p.Thr288Asn
NM_001191320.2:c.608C>A	NP_001178249.1:p.Thr203Asn
NM_001278631.2:c.608C>A	NP_001265560.1:p.Thr203Asn