Canonical Allele Identifier: CA1866994135
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541929G= , CM000671.2:g.98541929G= GRCh38
NC_000009.11:g.101304211G= , CM000671.1:g.101304211G= GRCh37
NC_000009.10:g.100344032G= NCBI36
NG_016426.1:g.172269C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.574C= MANE Select ENSP00000259455.2:p.His192=
ENST00000637410.1:n.352C=
ENST00000637717.1:c.190C= ENSP00000490789.1:p.His64=
ENST00000259455.3:c.574C= ENSP00000259455.2:p.His192=
ENST00000477471.1:n.361C=
ENST00000634227.1:n.348C=
NM_005458.7:c.574C= NP_005449.5:p.His192=
XM_017015331.2:c.280C= XP_016870820.1:p.His94=
NM_005458.8:c.574C= MANE Select NP_005449.5:p.His192=