HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727855C>A , CM000679.2:g.82727855C>A | GRCh38 |
NC_000017.10:g.80685731C>A , CM000679.1:g.80685731C>A | GRCh37 |
NC_000017.9:g.78279020C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*684C>A MANE Select | ENSP00000269373.6:n.*684C>A | |
ENST00000269373.10:c.*684C>A | ENSP00000269373.6:n.*684C>A | |
ENST00000571594.1:c.53+688C>A | ENSP00000459751.1:n.53+688C>A | |
NM_024619.3:c.*684C>A | NP_078895.2:n.*684C>A | |
NR_046408.1:n.1792C>A | ||
XM_024450948.1:c.*684C>A | XP_024306716.1:n.*684C>A | |
NM_024619.4:c.*684C>A MANE Select | NP_078895.2:n.*684C>A | |
NR_046408.2:n.1792C>A |