HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727923G= , CM000679.2:g.82727923G= | GRCh38 |
NC_000017.10:g.80685799G= , CM000679.1:g.80685799G= | GRCh37 |
NC_000017.9:g.78279088G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*752G= MANE Select | ENSP00000269373.6:n.*752G= | |
ENST00000269373.10:c.*752G= | ENSP00000269373.6:n.*752G= | |
ENST00000571594.1:c.53+756G= | ENSP00000459751.1:n.53+756G= | |
NM_024619.3:c.*752G= | NP_078895.2:n.*752G= | |
NR_046408.1:n.1860G= | ||
XM_024450948.1:c.*752G= | XP_024306716.1:n.*752G= | |
NM_024619.4:c.*752G= MANE Select | NP_078895.2:n.*752G= | |
NR_046408.2:n.1860G= |