Canonical Allele Identifier: CA466526949
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304170A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541888A>T , CM000671.2:g.98541888A>T GRCh38
NC_000009.11:g.101304170A>T , CM000671.1:g.101304170A>T GRCh37
NC_000009.10:g.100343991A>T NCBI36
NG_016426.1:g.172310T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.615T>A MANE Select ENSP00000259455.2:p.Val205=
ENST00000637410.1:n.393T>A
ENST00000637717.1:c.231T>A ENSP00000490789.1:p.Val77=
ENST00000259455.3:c.615T>A ENSP00000259455.2:p.Val205=
ENST00000477471.1:n.402T>A
ENST00000634227.1:n.389T>A
NM_005458.7:c.615T>A NP_005449.5:p.Val205=
XM_017015331.2:c.321T>A XP_016870820.1:p.Val107=
NM_005458.8:c.615T>A MANE Select NP_005449.5:p.Val205=