Canonical Allele Identifier: CA362175275

Gene: GABRB2

Linked Data

• MyVariant Identifiers: chr5:g.160758021C>G (hg19) ; chr5:g.161331014C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161331014C>G , CM000667.2:g.161331014C>G	GRCh38
NC_000005.9:g.160758021C>G , CM000667.1:g.160758021C>G	GRCh37
NC_000005.8:g.160690599C>G	NCBI36
NG_047050.1:g.222111G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274547.7:c.946G>C	ENSP00000274547.2:p.Val316Leu
ENST00000393959.6:c.946G>C MANE Select	ENSP00000377531.1:p.Val316Leu
ENST00000674514.1:n.1028G>C
ENST00000675081.1:c.*405G>C	ENSP00000502207.1:n.*405G>C
ENST00000675303.1:c.946G>C	ENSP00000502748.1:p.Val316Leu
ENST00000675381.1:c.694G>C	ENSP00000501968.1:p.Val232Leu
ENST00000675746.1:c.196G>C	ENSP00000502391.1:p.Val66Leu
ENST00000675773.1:c.946G>C	ENSP00000502701.1:p.Val316Leu
ENST00000274547.6:c.946G>C	ENSP00000274547.2:p.Val316Leu
ENST00000353437.10:c.946G>C	ENSP00000274546.6:p.Val316Leu
ENST00000393959.5:c.946G>C	ENSP00000377531.1:p.Val316Leu
ENST00000517547.5:c.466G>C	ENSP00000429750.1:p.Val156Leu
ENST00000517901.5:c.757G>C	ENSP00000430532.1:p.Val253Leu
ENST00000520240.5:c.946G>C	ENSP00000429320.1:p.Val316Leu
ENST00000612710.1:c.757G>C	ENSP00000480066.1:p.Val253Leu
NM_000813.2:c.946G>C	NP_000804.1:p.Val316Leu
NM_021911.2:c.946G>C	NP_068711.1:p.Val316Leu
XM_011534501.1:c.196G>C	XP_011532803.1:p.Val66Leu
NM_000813.3:c.946G>C	NP_000804.1:p.Val316Leu
NM_001371727.1:c.946G>C MANE Select	NP_001358656.1:p.Val316Leu
NM_021911.3:c.946G>C	NP_068711.1:p.Val316Leu