Canonical Allele Identifier: CA466527066
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304311T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542029T>G , CM000671.2:g.98542029T>G GRCh38
NC_000009.11:g.101304311T>G , CM000671.1:g.101304311T>G GRCh37
NC_000009.10:g.100344132T>G NCBI36
NG_016426.1:g.172169A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.474A>C MANE Select ENSP00000259455.2:p.Ala158=
ENST00000637410.1:n.252A>C
ENST00000637717.1:c.90A>C ENSP00000490789.1:p.Ala30=
ENST00000638001.1:n.84A>C
ENST00000259455.3:c.474A>C ENSP00000259455.2:p.Ala158=
ENST00000477471.1:n.261A>C
ENST00000634227.1:n.248A>C
NM_005458.7:c.474A>C NP_005449.5:p.Ala158=
XM_017015331.2:c.180A>C XP_016870820.1:p.Ala60=
NM_005458.8:c.474A>C MANE Select NP_005449.5:p.Ala158=