Canonical Allele Identifier: CA1866959937
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380699C= , CM000671.2:g.98380699C= GRCh38
NC_000009.11:g.101142981C= , CM000671.1:g.101142981C= GRCh37
NC_000009.10:g.100182802C= NCBI36
NG_016426.1:g.333499G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.1662+4941G= MANE Select ENSP00000259455.2:n.1662+4941G=
ENST00000637410.1:n.1440+4941G=
ENST00000259455.3:c.1662+4941G= ENSP00000259455.2:n.1662+4941G=
ENST00000634314.1:n.167+4941G=
NM_005458.7:c.1662+4941G= NP_005449.5:n.1662+4941G=
XM_005252316.3:c.888+4941G= XP_005252373.1:n.888+4941G=
XM_005252316.5:c.888+4941G= XP_005252373.1:n.888+4941G=
XM_017015331.2:c.1368+4941G= XP_016870820.1:n.1368+4941G=
XM_017015332.2:c.888+4941G= XP_016870821.1:n.888+4941G=
NM_005458.8:c.1662+4941G= MANE Select NP_005449.5:n.1662+4941G=
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