HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727563T>G , CM000679.2:g.82727563T>G | GRCh38 |
NC_000017.10:g.80685439T>G , CM000679.1:g.80685439T>G | GRCh37 |
NC_000017.9:g.78278728T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*392T>G MANE Select | ENSP00000269373.6:n.*392T>G | |
ENST00000269373.10:c.*392T>G | ENSP00000269373.6:n.*392T>G | |
ENST00000571594.1:c.53+396T>G | ENSP00000459751.1:n.53+396T>G | |
NM_024619.3:c.*392T>G | NP_078895.2:n.*392T>G | |
NR_046408.1:n.1500T>G | ||
XM_024450948.1:c.*392T>G | XP_024306716.1:n.*392T>G | |
NM_024619.4:c.*392T>G MANE Select | NP_078895.2:n.*392T>G | |
NR_046408.2:n.1500T>G |