Canonical Allele Identifier: CA1866959722
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380498G= , CM000671.2:g.98380498G= GRCh38
NC_000009.11:g.101142780G= , CM000671.1:g.101142780G= GRCh37
NC_000009.10:g.100182601G= NCBI36
NG_016426.1:g.333700C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.1662+5142C= MANE Select ENSP00000259455.2:n.1662+5142C=
ENST00000637410.1:n.1440+5142C=
ENST00000259455.3:c.1662+5142C= ENSP00000259455.2:n.1662+5142C=
ENST00000634314.1:n.167+5142C=
NM_005458.7:c.1662+5142C= NP_005449.5:n.1662+5142C=
XM_005252316.3:c.888+5142C= XP_005252373.1:n.888+5142C=
XM_005252316.5:c.888+5142C= XP_005252373.1:n.888+5142C=
XM_017015331.2:c.1368+5142C= XP_016870820.1:n.1368+5142C=
XM_017015332.2:c.888+5142C= XP_016870821.1:n.888+5142C=
NM_005458.8:c.1662+5142C= MANE Select NP_005449.5:n.1662+5142C=
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