Canonical Allele Identifier: CA466527053
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304302A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542020A>C , CM000671.2:g.98542020A>C GRCh38
NC_000009.11:g.101304302A>C , CM000671.1:g.101304302A>C GRCh37
NC_000009.10:g.100344123A>C NCBI36
NG_016426.1:g.172178T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.483T>G MANE Select ENSP00000259455.2:p.Pro161=
ENST00000637410.1:n.261T>G
ENST00000637717.1:c.99T>G ENSP00000490789.1:p.Pro33=
ENST00000638001.1:n.93T>G
ENST00000259455.3:c.483T>G ENSP00000259455.2:p.Pro161=
ENST00000477471.1:n.270T>G
ENST00000634227.1:n.257T>G
NM_005458.7:c.483T>G NP_005449.5:p.Pro161=
XM_017015331.2:c.189T>G XP_016870820.1:p.Pro63=
NM_005458.8:c.483T>G MANE Select NP_005449.5:p.Pro161=
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