Canonical Allele Identifier: CA466527063
Gene: GABBR2 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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