HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20576889A>G , CM000686.2:g.20576889A>G | GRCh38 |
NC_000024.9:g.22738775A>G , CM000686.1:g.22738775A>G | GRCh37 |
NC_000024.8:g.21148163A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361365.7:c.16+1002A>G MANE Select | ENSP00000354722.2:n.16+1002A>G | |
ENST00000361365.6:c.16+1002A>G | ENSP00000354722.2:n.16+1002A>G | |
ENST00000382772.3:c.16+1002A>G | ENSP00000372222.3:n.16+1002A>G | |
ENST00000465253.1:n.110+1002A>G | ||
NM_001278612.1:c.16+1002A>G | NP_001265541.1:n.16+1002A>G | |
NM_004681.3:c.16+1002A>G | NP_004672.2:n.16+1002A>G | |
NM_004681.4:c.16+1002A>G MANE Select | NP_004672.2:n.16+1002A>G | |
NM_001278612.2:c.16+1002A>G | NP_001265541.1:n.16+1002A>G |