HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38675866C= , CM000685.2:g.38675866C= | GRCh38 |
NC_000023.10:g.38535120C= , CM000685.1:g.38535120C= | GRCh37 |
NC_000023.9:g.38420064C= | NCBI36 |
NG_009160.1:g.119390C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378482.7:c.597+6C= MANE Select | ENSP00000367743.2:n.597+6C= | |
ENST00000286824.6:c.648+6C= | ENSP00000286824.6:n.648+6C= | |
ENST00000378482.6:c.597+6C= | ENSP00000367743.2:n.597+6C= | |
ENST00000419600.3:n.541+6C= | ||
ENST00000465127.1:c.687+6C= | ENSP00000417050.1:n.687+6C= | |
ENST00000471410.5:c.*623+6C= | ENSP00000419290.1:n.*623+6C= | |
ENST00000475216.5:c.*590+6C= | ENSP00000418586.1:n.*590+6C= | |
NM_004615.3:c.597+6C= | NP_004606.2:n.597+6C= | |
NM_004615.4:c.597+6C= MANE Select | NP_004606.2:n.597+6C= |