Canonical Allele Identifier: CA374351159
Gene: GABBR2 HGNC NCBI

Linked Data

COSMIC: COSM1103137
MyVariant Identifiers: chr9:g.101304300A>C (hg19) chr9:g.98542018A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542018A>C , CM000671.2:g.98542018A>C GRCh38
NC_000009.11:g.101304300A>C , CM000671.1:g.101304300A>C GRCh37
NC_000009.10:g.100344121A>C NCBI36
NG_016426.1:g.172180T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.485T>G MANE Select ENSP00000259455.2:p.Val162Gly
ENST00000637410.1:n.263T>G
ENST00000637717.1:c.101T>G ENSP00000490789.1:p.Val34Gly
ENST00000638001.1:n.95T>G
ENST00000259455.3:c.485T>G ENSP00000259455.2:p.Val162Gly
ENST00000477471.1:n.272T>G
ENST00000634227.1:n.259T>G
NM_005458.7:c.485T>G NP_005449.5:p.Val162Gly
XM_017015331.2:c.191T>G XP_016870820.1:p.Val64Gly
NM_005458.8:c.485T>G MANE Select NP_005449.5:p.Val162Gly
Search 100 bp 5'
Search 100 bp 3'