Canonical Allele Identifier: CA1866993951
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541678C= , CM000671.2:g.98541678C= GRCh38
NC_000009.11:g.101303960C= , CM000671.1:g.101303960C= GRCh37
NC_000009.10:g.100343781C= NCBI36
NG_016426.1:g.172520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+195G= MANE Select ENSP00000259455.2:n.630+195G=
ENST00000637410.1:n.408+195G=
ENST00000259455.3:c.630+195G= ENSP00000259455.2:n.630+195G=
ENST00000477471.1:n.417+195G=
ENST00000634227.1:n.404+195G=
NM_005458.7:c.630+195G= NP_005449.5:n.630+195G=
XM_017015331.2:c.336+195G= XP_016870820.1:n.336+195G=
NM_005458.8:c.630+195G= MANE Select NP_005449.5:n.630+195G=
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