Canonical Allele Identifier: CA1866927788
Gene: GABBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98442962T= , CM000671.2:g.98442962T= GRCh38
NC_000009.11:g.101205244T= , CM000671.1:g.101205244T= GRCh37
NC_000009.10:g.100245065T= NCBI36
NG_016426.1:g.271236A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.1236+11019A= MANE Select ENSP00000259455.2:n.1236+11019A=
ENST00000637410.1:n.1014+11019A=
ENST00000259455.3:c.1236+11019A= ENSP00000259455.2:n.1236+11019A=
NM_005458.7:c.1236+11019A= NP_005449.5:n.1236+11019A=
XM_005252316.3:c.462+11019A= XP_005252373.1:n.462+11019A=
XM_005252316.5:c.462+11019A= XP_005252373.1:n.462+11019A=
XM_017015331.2:c.942+11019A= XP_016870820.1:n.942+11019A=
XM_017015332.2:c.462+11019A= XP_016870821.1:n.462+11019A=
NM_005458.8:c.1236+11019A= MANE Select NP_005449.5:n.1236+11019A=
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