Canonical Allele Identifier: CA391462170

Gene: GABRB3

Linked Data

• MyVariant Identifiers: chr15:g.26806259G>C (hg19) ; chr15:g.26561112G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.26561112G>C , CM000677.2:g.26561112G>C	GRCh38
NC_000015.9:g.26806259G>C , CM000677.1:g.26806259G>C	GRCh37
NC_000015.8:g.24357352G>C	NCBI36
NG_012836.1:g.217669C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299267.9:c.900C>G	ENSP00000299267.4:p.Ile300Met
ENST00000311550.10:c.900C>G MANE Select	ENSP00000308725.5:p.Ile300Met
ENST00000635832.1:n.943C>G
ENST00000635994.1:c.583C>G
ENST00000636466.1:c.645C>G	ENSP00000489768.1:p.Ile215Met
ENST00000638099.1:c.801C>G	ENSP00000490678.1:p.Ile267Met
ENST00000299267.8:c.900C>G	ENSP00000299267.4:p.Ile300Met
ENST00000311550.9:c.900C>G	ENSP00000308725.5:p.Ile300Met
ENST00000400188.7:c.687C>G	ENSP00000383049.3:p.Ile229Met
ENST00000541819.6:c.1068C>G	ENSP00000442408.2:p.Ile356Met
ENST00000545868.4:c.645C>G	ENSP00000439169.1:p.Ile215Met
ENST00000554556.5:c.*361C>G	ENSP00000451077.1:n.*361C>G
ENST00000555094.5:n.812C>G
ENST00000555632.5:c.*732C>G	ENSP00000452041.1:n.*732C>G
ENST00000622697.4:c.645C>G	ENSP00000481004.1:p.Ile215Met
ENST00000628124.2:c.645C>G	ENSP00000486819.1:p.Ile215Met
NM_000814.5:c.900C>G	NP_000805.1:p.Ile300Met
NM_001191320.1:c.645C>G	NP_001178249.1:p.Ile215Met
NM_001191321.2:c.687C>G	NP_001178250.1:p.Ile229Met
NM_001278631.1:c.645C>G	NP_001265560.1:p.Ile215Met
NM_021912.4:c.900C>G	NP_068712.1:p.Ile300Met
XM_011521428.1:c.723C>G	XP_011519730.1:p.Ile241Met
XM_011521428.3:c.723C>G	XP_011519730.1:p.Ile241Met
NM_000814.6:c.900C>G MANE Select	NP_000805.1:p.Ile300Met
NM_001191321.3:c.687C>G	NP_001178250.1:p.Ile229Met
NM_021912.5:c.900C>G	NP_068712.1:p.Ile300Met
NM_001191320.2:c.645C>G	NP_001178249.1:p.Ile215Met
NM_001278631.2:c.645C>G	NP_001265560.1:p.Ile215Met