| HGVS | Genome Assembly | 
|---|---|
| NC_000005.10:g.161548936T>G , CM000667.2:g.161548936T>G | GRCh38 | 
| NC_000005.9:g.160975942T>G , CM000667.1:g.160975942T>G | GRCh37 | 
| NC_000005.8:g.160908520T>G | NCBI36 | 
| NG_047050.1:g.4189A>C | 
| HGVS | Amino-acid Change | 
|---|---|
| ENST00000522269.5:n.41+1833T>G (GABRA6) | |
| ENST00000523730.1:n.109A>C (GABRB2) |