Canonical Allele Identifier: CA1866994182
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541996G= , CM000671.2:g.98541996G= GRCh38
NC_000009.11:g.101304278G= , CM000671.1:g.101304278G= GRCh37
NC_000009.10:g.100344099G= NCBI36
NG_016426.1:g.172202C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.507C= MANE Select ENSP00000259455.2:p.Tyr169=
ENST00000637410.1:n.285C=
ENST00000637717.1:c.123C= ENSP00000490789.1:p.Tyr41=
ENST00000259455.3:c.507C= ENSP00000259455.2:p.Tyr169=
ENST00000477471.1:n.294C=
ENST00000634227.1:n.281C=
NM_005458.7:c.507C= NP_005449.5:p.Tyr169=
XM_017015331.2:c.213C= XP_016870820.1:p.Tyr71=
NM_005458.8:c.507C= MANE Select NP_005449.5:p.Tyr169=