Canonical Allele Identifier: CA374351113
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304280A>C (hg19) chr9:g.98541998A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541998A>C , CM000671.2:g.98541998A>C GRCh38
NC_000009.11:g.101304280A>C , CM000671.1:g.101304280A>C GRCh37
NC_000009.10:g.100344101A>C NCBI36
NG_016426.1:g.172200T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.505T>G MANE Select ENSP00000259455.2:p.Tyr169Asp
ENST00000637410.1:n.283T>G
ENST00000637717.1:c.121T>G ENSP00000490789.1:p.Tyr41Asp
ENST00000259455.3:c.505T>G ENSP00000259455.2:p.Tyr169Asp
ENST00000477471.1:n.292T>G
ENST00000634227.1:n.279T>G
NM_005458.7:c.505T>G NP_005449.5:p.Tyr169Asp
XM_017015331.2:c.211T>G XP_016870820.1:p.Tyr71Asp
NM_005458.8:c.505T>G MANE Select NP_005449.5:p.Tyr169Asp
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