Canonical Allele Identifier: CA1867008046
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515206G= , CM000671.2:g.98515206G= GRCh38
NC_000009.11:g.101277488G= , CM000671.1:g.101277488G= GRCh37
NC_000009.10:g.100317309G= NCBI36
NG_016426.1:g.198992C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.631-18692C= MANE Select ENSP00000259455.2:n.631-18692C=
ENST00000637410.1:n.409-18692C=
ENST00000259455.3:c.631-18692C= ENSP00000259455.2:n.631-18692C=
ENST00000477471.1:n.418-18692C=
ENST00000634227.1:n.405-18692C=
ENST00000634919.1:n.306+788C=
NM_005458.7:c.631-18692C= NP_005449.5:n.631-18692C=
XM_005252316.3:c.-144-18692C= XP_005252373.1:n.-144-18692C=
XM_005252316.5:c.-144-18692C= XP_005252373.1:n.-144-18692C=
XM_017015331.2:c.337-18692C= XP_016870820.1:n.337-18692C=
NM_005458.8:c.631-18692C= MANE Select NP_005449.5:n.631-18692C=