Canonical Allele Identifier: CA1866959788
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380554G= , CM000671.2:g.98380554G= GRCh38
NC_000009.11:g.101142836G= , CM000671.1:g.101142836G= GRCh37
NC_000009.10:g.100182657G= NCBI36
NG_016426.1:g.333644C=

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5086C= MANE Select ENSP00000259455.2:n.1662+5086C=
ENST00000637410.1:n.1440+5086C=
ENST00000259455.3:c.1662+5086C= ENSP00000259455.2:n.1662+5086C=
ENST00000634314.1:n.167+5086C=
NM_005458.7:c.1662+5086C= NP_005449.5:n.1662+5086C=
XM_005252316.3:c.888+5086C= XP_005252373.1:n.888+5086C=
XM_005252316.5:c.888+5086C= XP_005252373.1:n.888+5086C=
XM_017015331.2:c.1368+5086C= XP_016870820.1:n.1368+5086C=
XM_017015332.2:c.888+5086C= XP_016870821.1:n.888+5086C=
NM_005458.8:c.1662+5086C= MANE Select NP_005449.5:n.1662+5086C=
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