Canonical Allele Identifier: CA466527062
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304308G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542026G>A , CM000671.2:g.98542026G>A GRCh38
NC_000009.11:g.101304308G>A , CM000671.1:g.101304308G>A GRCh37
NC_000009.10:g.100344129G>A NCBI36
NG_016426.1:g.172172C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.477C>T MANE Select ENSP00000259455.2:p.Thr159=
ENST00000637410.1:n.255C>T
ENST00000637717.1:c.93C>T ENSP00000490789.1:p.Thr31=
ENST00000638001.1:n.87C>T
ENST00000259455.3:c.477C>T ENSP00000259455.2:p.Thr159=
ENST00000477471.1:n.264C>T
ENST00000634227.1:n.251C>T
NM_005458.7:c.477C>T NP_005449.5:p.Thr159=
XM_017015331.2:c.183C>T XP_016870820.1:p.Thr61=
NM_005458.8:c.477C>T MANE Select NP_005449.5:p.Thr159=