Canonical Allele Identifier: CA1866993871
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541599A= , CM000671.2:g.98541599A= GRCh38
NC_000009.11:g.101303881A= , CM000671.1:g.101303881A= GRCh37
NC_000009.10:g.100343702A= NCBI36
NG_016426.1:g.172599T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+274T= MANE Select ENSP00000259455.2:n.630+274T=
ENST00000637410.1:n.408+274T=
ENST00000259455.3:c.630+274T= ENSP00000259455.2:n.630+274T=
ENST00000477471.1:n.417+274T=
ENST00000634227.1:n.404+274T=
NM_005458.7:c.630+274T= NP_005449.5:n.630+274T=
XM_017015331.2:c.336+274T= XP_016870820.1:n.336+274T=
NM_005458.8:c.630+274T= MANE Select NP_005449.5:n.630+274T=