Canonical Allele Identifier: CA1866993987
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541720A= , CM000671.2:g.98541720A= GRCh38
NC_000009.11:g.101304002A= , CM000671.1:g.101304002A= GRCh37
NC_000009.10:g.100343823A= NCBI36
NG_016426.1:g.172478T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+153T= MANE Select ENSP00000259455.2:n.630+153T=
ENST00000637410.1:n.408+153T=
ENST00000259455.3:c.630+153T= ENSP00000259455.2:n.630+153T=
ENST00000477471.1:n.417+153T=
ENST00000634227.1:n.404+153T=
NM_005458.7:c.630+153T= NP_005449.5:n.630+153T=
XM_017015331.2:c.336+153T= XP_016870820.1:n.336+153T=
NM_005458.8:c.630+153T= MANE Select NP_005449.5:n.630+153T=