HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727695G= , CM000679.2:g.82727695G= | GRCh38 |
NC_000017.10:g.80685571G= , CM000679.1:g.80685571G= | GRCh37 |
NC_000017.9:g.78278860G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*524G= MANE Select | ENSP00000269373.6:n.*524G= | |
ENST00000269373.10:c.*524G= | ENSP00000269373.6:n.*524G= | |
ENST00000571594.1:c.53+528G= | ENSP00000459751.1:n.53+528G= | |
NM_024619.3:c.*524G= | NP_078895.2:n.*524G= | |
NR_046408.1:n.1632G= | ||
XM_024450948.1:c.*524G= | XP_024306716.1:n.*524G= | |
NM_024619.4:c.*524G= MANE Select | NP_078895.2:n.*524G= | |
NR_046408.2:n.1632G= |