Canonical Allele Identifier: CA362175464
Community Standard Title: NM_001371727.1(GABRB2):c.860C>T (p.Thr287Ile)
Gene: GABRB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161331100G>A , CM000667.2:g.161331100G>A GRCh38
NC_000005.9:g.160758107G>A , CM000667.1:g.160758107G>A GRCh37
NC_000005.8:g.160690685G>A NCBI36
NG_047050.1:g.222025C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001371727.1:c.860C>T MANE Select NP_001358656.1:p.Thr287Ile
ENST00000393959.6:c.860C>T MANE Select ENSP00000377531.1:p.Thr287Ile
NM_000813.2:c.860C>T NP_000804.1:p.Thr287Ile
NM_000813.3:c.860C>T NP_000804.1:p.Thr287Ile
NM_021911.2:c.860C>T NP_068711.1:p.Thr287Ile
NM_021911.3:c.860C>T NP_068711.1:p.Thr287Ile
ENST00000274547.6:c.860C>T ENSP00000274547.2:p.Thr287Ile
ENST00000274547.7:c.860C>T ENSP00000274547.2:p.Thr287Ile
ENST00000353437.10:c.860C>T ENSP00000274546.6:p.Thr287Ile
ENST00000393959.5:c.860C>T ENSP00000377531.1:p.Thr287Ile
ENST00000517547.5:c.380C>T ENSP00000429750.1:p.Thr127Ile
ENST00000517901.5:c.671C>T ENSP00000430532.1:p.Thr224Ile
ENST00000520240.5:c.860C>T ENSP00000429320.1:p.Thr287Ile
ENST00000612710.1:c.671C>T ENSP00000480066.1:p.Thr224Ile
ENST00000674514.1:n.942C>T
ENST00000675081.1:c.*319C>T ENSP00000502207.1:n.*319C>T
ENST00000675303.1:c.860C>T ENSP00000502748.1:p.Thr287Ile
ENST00000675381.1:c.608C>T ENSP00000501968.1:p.Thr203Ile
ENST00000675746.1:c.110C>T ENSP00000502391.1:p.Thr37Ile
ENST00000675773.1:c.860C>T ENSP00000502701.1:p.Thr287Ile
XM_011534501.1:c.110C>T XP_011532803.1:p.Thr37Ile