HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888234A>G , CM000684.2:g.20888234A>G | GRCh38 |
NC_000022.10:g.21242522A>G , CM000684.1:g.21242522A>G | GRCh37 |
NC_000022.9:g.19572522A>G | NCBI36 |
NG_012152.1:g.34231A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*398A>G MANE Select | ENSP00000215730.6:n.*398A>G | |
ENST00000215730.11:c.*398A>G | ENSP00000215730.6:n.*398A>G | |
NM_004782.3:c.*398A>G | NP_004773.1:n.*398A>G | |
NM_004782.4:c.*398A>G MANE Select | NP_004773.1:n.*398A>G |