Canonical Allele Identifier: CA362175328

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160758044T>C (hg19) ; chr5:g.161331037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161331037T>C , CM000667.2:g.161331037T>C	GRCh38
NC_000005.9:g.160758044T>C , CM000667.1:g.160758044T>C	GRCh37
NC_000005.8:g.160690622T>C	NCBI36
NG_047050.1:g.222088A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.923A>G	ENSP00000274547.2:p.Tyr308Cys
ENST00000393959.6:c.923A>G MANE Select	ENSP00000377531.1:p.Tyr308Cys
ENST00000674514.1:n.1005A>G
ENST00000675081.1:c.*382A>G	ENSP00000502207.1:n.*382A>G
ENST00000675303.1:c.923A>G	ENSP00000502748.1:p.Tyr308Cys
ENST00000675381.1:c.671A>G	ENSP00000501968.1:p.Tyr224Cys
ENST00000675746.1:c.173A>G	ENSP00000502391.1:p.Tyr58Cys
ENST00000675773.1:c.923A>G	ENSP00000502701.1:p.Tyr308Cys
ENST00000274547.6:c.923A>G	ENSP00000274547.2:p.Tyr308Cys
ENST00000353437.10:c.923A>G	ENSP00000274546.6:p.Tyr308Cys
ENST00000393959.5:c.923A>G	ENSP00000377531.1:p.Tyr308Cys
ENST00000517547.5:c.443A>G	ENSP00000429750.1:p.Tyr148Cys
ENST00000517901.5:c.734A>G	ENSP00000430532.1:p.Tyr245Cys
ENST00000520240.5:c.923A>G	ENSP00000429320.1:p.Tyr308Cys
ENST00000612710.1:c.734A>G	ENSP00000480066.1:p.Tyr245Cys
NM_000813.2:c.923A>G	NP_000804.1:p.Tyr308Cys
NM_021911.2:c.923A>G	NP_068711.1:p.Tyr308Cys
XM_011534501.1:c.173A>G	XP_011532803.1:p.Tyr58Cys
NM_000813.3:c.923A>G	NP_000804.1:p.Tyr308Cys
NM_001371727.1:c.923A>G MANE Select	NP_001358656.1:p.Tyr308Cys
NM_021911.3:c.923A>G	NP_068711.1:p.Tyr308Cys