Canonical Allele Identifier: CA362175169

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160757976A>C (hg19) ; chr5:g.161330969A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161330969A>C , CM000667.2:g.161330969A>C	GRCh38
NC_000005.9:g.160757976A>C , CM000667.1:g.160757976A>C	GRCh37
NC_000005.8:g.160690554A>C	NCBI36
NG_047050.1:g.222156T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.991T>G	ENSP00000274547.2:p.Phe331Val
ENST00000393959.6:c.991T>G MANE Select	ENSP00000377531.1:p.Phe331Val
ENST00000674514.1:n.1073T>G
ENST00000675081.1:c.*450T>G	ENSP00000502207.1:n.*450T>G
ENST00000675303.1:c.991T>G	ENSP00000502748.1:p.Phe331Val
ENST00000675381.1:c.739T>G	ENSP00000501968.1:p.Phe247Val
ENST00000675746.1:c.241T>G	ENSP00000502391.1:p.Phe81Val
ENST00000675773.1:c.991T>G	ENSP00000502701.1:p.Phe331Val
ENST00000274547.6:c.991T>G	ENSP00000274547.2:p.Phe331Val
ENST00000353437.10:c.991T>G	ENSP00000274546.6:p.Phe331Val
ENST00000393959.5:c.991T>G	ENSP00000377531.1:p.Phe331Val
ENST00000517547.5:c.511T>G	ENSP00000429750.1:p.Phe171Val
ENST00000517901.5:c.802T>G	ENSP00000430532.1:p.Phe268Val
ENST00000520240.5:c.991T>G	ENSP00000429320.1:p.Phe331Val
ENST00000612710.1:c.802T>G	ENSP00000480066.1:p.Phe268Val
NM_000813.2:c.991T>G	NP_000804.1:p.Phe331Val
NM_021911.2:c.991T>G	NP_068711.1:p.Phe331Val
XM_011534501.1:c.241T>G	XP_011532803.1:p.Phe81Val
NM_000813.3:c.991T>G	NP_000804.1:p.Phe331Val
NM_001371727.1:c.991T>G MANE Select	NP_001358656.1:p.Phe331Val
NM_021911.3:c.991T>G	NP_068711.1:p.Phe331Val