Canonical Allele Identifier: CA1866994235
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542024G= , CM000671.2:g.98542024G= GRCh38
NC_000009.11:g.101304306G= , CM000671.1:g.101304306G= GRCh37
NC_000009.10:g.100344127G= NCBI36
NG_016426.1:g.172174C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.479C= MANE Select ENSP00000259455.2:p.Thr160=
ENST00000637410.1:n.257C=
ENST00000637717.1:c.95C= ENSP00000490789.1:p.Thr32=
ENST00000638001.1:n.89C=
ENST00000259455.3:c.479C= ENSP00000259455.2:p.Thr160=
ENST00000477471.1:n.266C=
ENST00000634227.1:n.253C=
NM_005458.7:c.479C= NP_005449.5:p.Thr160=
XM_017015331.2:c.185C= XP_016870820.1:p.Thr62=
NM_005458.8:c.479C= MANE Select NP_005449.5:p.Thr160=