Canonical Allele Identifier: CA1866994442
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542212G= , CM000671.2:g.98542212G= GRCh38
NC_000009.11:g.101304494G= , CM000671.1:g.101304494G= GRCh37
NC_000009.10:g.100344315G= NCBI36
NG_016426.1:g.171986C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.460-169C= MANE Select ENSP00000259455.2:n.460-169C=
ENST00000637410.1:n.238-169C=
ENST00000637717.1:c.76-169C= ENSP00000490789.1:n.76-169C=
ENST00000638001.1:n.70-169C=
ENST00000259455.3:c.460-169C= ENSP00000259455.2:n.460-169C=
ENST00000477471.1:n.247-169C=
ENST00000634227.1:n.234-169C=
NM_005458.7:c.460-169C= NP_005449.5:n.460-169C=
XM_017015331.2:c.166-169C= XP_016870820.1:n.166-169C=
NM_005458.8:c.460-169C= MANE Select NP_005449.5:n.460-169C=
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