Canonical Allele Identifier: CA374351194
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304318A>C (hg19) chr9:g.98542036A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542036A>C , CM000671.2:g.98542036A>C GRCh38
NC_000009.11:g.101304318A>C , CM000671.1:g.101304318A>C GRCh37
NC_000009.10:g.100344139A>C NCBI36
NG_016426.1:g.172162T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.467T>G MANE Select ENSP00000259455.2:p.Phe156Cys
ENST00000637410.1:n.245T>G
ENST00000637717.1:c.83T>G ENSP00000490789.1:p.Phe28Cys
ENST00000638001.1:n.77T>G
ENST00000259455.3:c.467T>G ENSP00000259455.2:p.Phe156Cys
ENST00000477471.1:n.254T>G
ENST00000634227.1:n.241T>G
NM_005458.7:c.467T>G NP_005449.5:p.Phe156Cys
XM_017015331.2:c.173T>G XP_016870820.1:p.Phe58Cys
NM_005458.8:c.467T>G MANE Select NP_005449.5:p.Phe156Cys
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