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) |