Canonical Allele Identifier: CA466526942
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304158A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541876A>T , CM000671.2:g.98541876A>T GRCh38
NC_000009.11:g.101304158A>T , CM000671.1:g.101304158A>T GRCh37
NC_000009.10:g.100343979A>T NCBI36
NG_016426.1:g.172322T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.627T>A MANE Select ENSP00000259455.2:p.Ser209=
ENST00000637410.1:n.405T>A
ENST00000259455.3:c.627T>A ENSP00000259455.2:p.Ser209=
ENST00000477471.1:n.414T>A
ENST00000634227.1:n.401T>A
NM_005458.7:c.627T>A NP_005449.5:p.Ser209=
XM_017015331.2:c.333T>A XP_016870820.1:p.Ser111=
NM_005458.8:c.627T>A MANE Select NP_005449.5:p.Ser209=