Canonical Allele Identifier: CA362175184

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160757982T>A (hg19) ; chr5:g.161330975T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161330975T>A , CM000667.2:g.161330975T>A	GRCh38
NC_000005.9:g.160757982T>A , CM000667.1:g.160757982T>A	GRCh37
NC_000005.8:g.160690560T>A	NCBI36
NG_047050.1:g.222150A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.985A>T	ENSP00000274547.2:p.Ile329Phe
ENST00000393959.6:c.985A>T MANE Select	ENSP00000377531.1:p.Ile329Phe
ENST00000674514.1:n.1067A>T
ENST00000675081.1:c.*444A>T	ENSP00000502207.1:n.*444A>T
ENST00000675303.1:c.985A>T	ENSP00000502748.1:p.Ile329Phe
ENST00000675381.1:c.733A>T	ENSP00000501968.1:p.Ile245Phe
ENST00000675746.1:c.235A>T	ENSP00000502391.1:p.Ile79Phe
ENST00000675773.1:c.985A>T	ENSP00000502701.1:p.Ile329Phe
ENST00000274547.6:c.985A>T	ENSP00000274547.2:p.Ile329Phe
ENST00000353437.10:c.985A>T	ENSP00000274546.6:p.Ile329Phe
ENST00000393959.5:c.985A>T	ENSP00000377531.1:p.Ile329Phe
ENST00000517547.5:c.505A>T	ENSP00000429750.1:p.Ile169Phe
ENST00000517901.5:c.796A>T	ENSP00000430532.1:p.Ile266Phe
ENST00000520240.5:c.985A>T	ENSP00000429320.1:p.Ile329Phe
ENST00000612710.1:c.796A>T	ENSP00000480066.1:p.Ile266Phe
NM_000813.2:c.985A>T	NP_000804.1:p.Ile329Phe
NM_021911.2:c.985A>T	NP_068711.1:p.Ile329Phe
XM_011534501.1:c.235A>T	XP_011532803.1:p.Ile79Phe
NM_000813.3:c.985A>T	NP_000804.1:p.Ile329Phe
NM_001371727.1:c.985A>T MANE Select	NP_001358656.1:p.Ile329Phe
NM_021911.3:c.985A>T	NP_068711.1:p.Ile329Phe