Canonical Allele Identifier: CA466527037
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304287C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98542005C>T , CM000671.2:g.98542005C>T GRCh38
NC_000009.11:g.101304287C>T , CM000671.1:g.101304287C>T GRCh37
NC_000009.10:g.100344108C>T NCBI36
NG_016426.1:g.172193G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.498G>A MANE Select ENSP00000259455.2:p.Lys166=
ENST00000637410.1:n.276G>A
ENST00000637717.1:c.114G>A ENSP00000490789.1:p.Lys38=
ENST00000259455.3:c.498G>A ENSP00000259455.2:p.Lys166=
ENST00000477471.1:n.285G>A
ENST00000634227.1:n.272G>A
NM_005458.7:c.498G>A NP_005449.5:p.Lys166=
XM_017015331.2:c.204G>A XP_016870820.1:p.Lys68=
NM_005458.8:c.498G>A MANE Select NP_005449.5:p.Lys166=