Canonical Allele Identifier: CA1866994063
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541839T= , CM000671.2:g.98541839T= GRCh38
NC_000009.11:g.101304121T= , CM000671.1:g.101304121T= GRCh37
NC_000009.10:g.100343942T= NCBI36
NG_016426.1:g.172359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+34A= MANE Select ENSP00000259455.2:n.630+34A=
ENST00000637410.1:n.408+34A=
ENST00000259455.3:c.630+34A= ENSP00000259455.2:n.630+34A=
ENST00000477471.1:n.417+34A=
ENST00000634227.1:n.404+34A=
NM_005458.7:c.630+34A= NP_005449.5:n.630+34A=
XM_017015331.2:c.336+34A= XP_016870820.1:n.336+34A=
NM_005458.8:c.630+34A= MANE Select NP_005449.5:n.630+34A=