Canonical Allele Identifier: CA1867008080
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515250T= , CM000671.2:g.98515250T= GRCh38
NC_000009.11:g.101277532T= , CM000671.1:g.101277532T= GRCh37
NC_000009.10:g.100317353T= NCBI36
NG_016426.1:g.198948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.631-18736A= MANE Select ENSP00000259455.2:n.631-18736A=
ENST00000637410.1:n.409-18736A=
ENST00000259455.3:c.631-18736A= ENSP00000259455.2:n.631-18736A=
ENST00000477471.1:n.418-18736A=
ENST00000634227.1:n.405-18736A=
ENST00000634919.1:n.306+744A=
NM_005458.7:c.631-18736A= NP_005449.5:n.631-18736A=
XM_005252316.3:c.-144-18736A= XP_005252373.1:n.-144-18736A=
XM_005252316.5:c.-144-18736A= XP_005252373.1:n.-144-18736A=
XM_017015331.2:c.337-18736A= XP_016870820.1:n.337-18736A=
NM_005458.8:c.631-18736A= MANE Select NP_005449.5:n.631-18736A=