Canonical Allele Identifier: CA1866994158
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541969T= , CM000671.2:g.98541969T= GRCh38
NC_000009.11:g.101304251T= , CM000671.1:g.101304251T= GRCh37
NC_000009.10:g.100344072T= NCBI36
NG_016426.1:g.172229A=

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.534A= MANE Select ENSP00000259455.2:p.Ser178=
ENST00000637410.1:n.312A=
ENST00000637717.1:c.150A= ENSP00000490789.1:p.Ser50=
ENST00000259455.3:c.534A= ENSP00000259455.2:p.Ser178=
ENST00000477471.1:n.321A=
ENST00000634227.1:n.308A=
NM_005458.7:c.534A= NP_005449.5:p.Ser178=
XM_017015331.2:c.240A= XP_016870820.1:p.Ser80=
NM_005458.8:c.534A= MANE Select NP_005449.5:p.Ser178=