Canonical Allele Identifier: CA1866993972
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541697G= , CM000671.2:g.98541697G= GRCh38
NC_000009.11:g.101303979G= , CM000671.1:g.101303979G= GRCh37
NC_000009.10:g.100343800G= NCBI36
NG_016426.1:g.172501C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+176C= MANE Select ENSP00000259455.2:n.630+176C=
ENST00000637410.1:n.408+176C=
ENST00000259455.3:c.630+176C= ENSP00000259455.2:n.630+176C=
ENST00000477471.1:n.417+176C=
ENST00000634227.1:n.404+176C=
NM_005458.7:c.630+176C= NP_005449.5:n.630+176C=
XM_017015331.2:c.336+176C= XP_016870820.1:n.336+176C=
NM_005458.8:c.630+176C= MANE Select NP_005449.5:n.630+176C=