HGVS | Genome Assembly |
---|---|
NC_000006.12:g.149287678C>G , CM000668.2:g.149287678C>G | GRCh38 |
NC_000006.11:g.149608814C>G , CM000668.1:g.149608814C>G | GRCh37 |
NC_000006.10:g.149650507C>G | NCBI36 |
NG_021386.2:g.74755C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000606202.1:c.-121+68902C>G | ENSP00000476139.1:n.-121+68902C>G | |
NM_001292035.2:c.6+68902C>G | NP_001278964.1:n.6+68902C>G | |
NM_001292035.3:c.6+68902C>G | NP_001278964.1:n.6+68902C>G |