Canonical Allele Identifier: CA1866994606
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542392T= , CM000671.2:g.98542392T= GRCh38
NC_000009.11:g.101304674T= , CM000671.1:g.101304674T= GRCh37
NC_000009.10:g.100344495T= NCBI36
NG_016426.1:g.171806A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-349A= MANE Select ENSP00000259455.2:n.460-349A=
ENST00000637410.1:n.238-349A=
ENST00000637717.1:c.76-349A= ENSP00000490789.1:n.76-349A=
ENST00000638001.1:n.70-349A=
ENST00000259455.3:c.460-349A= ENSP00000259455.2:n.460-349A=
ENST00000477471.1:n.247-349A=
ENST00000634227.1:n.234-349A=
NM_005458.7:c.460-349A= NP_005449.5:n.460-349A=
XM_017015331.2:c.166-349A= XP_016870820.1:n.166-349A=
NM_005458.8:c.460-349A= MANE Select NP_005449.5:n.460-349A=