Canonical Allele Identifier: CA391464078

Gene: GABRB3

Linked Data

• dbSNP Id: rs1235802940
• gnomAD v2: 15-26825547-T-C
• gnomAD v4: 15-26580400-T-C
• MyVariant Identifiers: chr15:g.26825547T>C (hg19) ; chr15:g.26580400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26580400T>C , CM000677.2:g.26580400T>C	GRCh38
NC_000015.9:g.26825547T>C , CM000677.1:g.26825547T>C	GRCh37
NC_000015.8:g.24376640T>C	NCBI36
NG_012836.1:g.198381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.601A>G	ENSP00000299267.4:p.Thr201Ala
ENST00000311550.10:c.601A>G MANE Select	ENSP00000308725.5:p.Thr201Ala
ENST00000635832.1:n.644A>G
ENST00000635994.1:c.284A>G
ENST00000636466.1:c.346A>G	ENSP00000489768.1:p.Thr116Ala
ENST00000638099.1:c.502A>G	ENSP00000490678.1:p.Thr168Ala
ENST00000299267.8:c.601A>G	ENSP00000299267.4:p.Thr201Ala
ENST00000311550.9:c.601A>G	ENSP00000308725.5:p.Thr201Ala
ENST00000400188.7:c.388A>G	ENSP00000383049.3:p.Thr130Ala
ENST00000541819.6:c.769A>G	ENSP00000442408.2:p.Thr257Ala
ENST00000545868.4:c.346A>G	ENSP00000439169.1:p.Thr116Ala
ENST00000554556.5:c.*62A>G	ENSP00000451077.1:n.*62A>G
ENST00000555094.5:n.513A>G
ENST00000555632.5:c.*433A>G	ENSP00000452041.1:n.*433A>G
ENST00000557765.1:n.272A>G
ENST00000622697.4:c.346A>G	ENSP00000481004.1:p.Thr116Ala
ENST00000628124.2:c.346A>G	ENSP00000486819.1:p.Thr116Ala
NM_000814.5:c.601A>G	NP_000805.1:p.Thr201Ala
NM_001191320.1:c.346A>G	NP_001178249.1:p.Thr116Ala
NM_001191321.2:c.388A>G	NP_001178250.1:p.Thr130Ala
NM_001278631.1:c.346A>G	NP_001265560.1:p.Thr116Ala
NM_021912.4:c.601A>G	NP_068712.1:p.Thr201Ala
XM_011521428.1:c.424A>G	XP_011519730.1:p.Thr142Ala
XM_011521428.3:c.424A>G	XP_011519730.1:p.Thr142Ala
NM_000814.6:c.601A>G MANE Select	NP_000805.1:p.Thr201Ala
NM_001191321.3:c.388A>G	NP_001178250.1:p.Thr130Ala
NM_021912.5:c.601A>G	NP_068712.1:p.Thr201Ala
NM_001191320.2:c.346A>G	NP_001178249.1:p.Thr116Ala
NM_001278631.2:c.346A>G	NP_001265560.1:p.Thr116Ala