Canonical Allele Identifier: CA1866993921
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541637A= , CM000671.2:g.98541637A= GRCh38
NC_000009.11:g.101303919A= , CM000671.1:g.101303919A= GRCh37
NC_000009.10:g.100343740A= NCBI36
NG_016426.1:g.172561T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+236T= MANE Select ENSP00000259455.2:n.630+236T=
ENST00000637410.1:n.408+236T=
ENST00000259455.3:c.630+236T= ENSP00000259455.2:n.630+236T=
ENST00000477471.1:n.417+236T=
ENST00000634227.1:n.404+236T=
NM_005458.7:c.630+236T= NP_005449.5:n.630+236T=
XM_017015331.2:c.336+236T= XP_016870820.1:n.336+236T=
NM_005458.8:c.630+236T= MANE Select NP_005449.5:n.630+236T=