Canonical Allele Identifier: CA466527013
Gene: GABBR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.101304263C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541981C>A , CM000671.2:g.98541981C>A GRCh38
NC_000009.11:g.101304263C>A , CM000671.1:g.101304263C>A GRCh37
NC_000009.10:g.100344084C>A NCBI36
NG_016426.1:g.172217G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.522G>T MANE Select ENSP00000259455.2:p.Arg174=
ENST00000637410.1:n.300G>T
ENST00000637717.1:c.138G>T ENSP00000490789.1:p.Arg46=
ENST00000259455.3:c.522G>T ENSP00000259455.2:p.Arg174=
ENST00000477471.1:n.309G>T
ENST00000634227.1:n.296G>T
NM_005458.7:c.522G>T NP_005449.5:p.Arg174=
XM_017015331.2:c.228G>T XP_016870820.1:p.Arg76=
NM_005458.8:c.522G>T MANE Select NP_005449.5:p.Arg174=