Canonical Allele Identifier: CA1866993885
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541607T= , CM000671.2:g.98541607T= GRCh38
NC_000009.11:g.101303889T= , CM000671.1:g.101303889T= GRCh37
NC_000009.10:g.100343710T= NCBI36
NG_016426.1:g.172591A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+266A= MANE Select ENSP00000259455.2:n.630+266A=
ENST00000637410.1:n.408+266A=
ENST00000259455.3:c.630+266A= ENSP00000259455.2:n.630+266A=
ENST00000477471.1:n.417+266A=
ENST00000634227.1:n.404+266A=
NM_005458.7:c.630+266A= NP_005449.5:n.630+266A=
XM_017015331.2:c.336+266A= XP_016870820.1:n.336+266A=
NM_005458.8:c.630+266A= MANE Select NP_005449.5:n.630+266A=
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