HGVS | Genome Assembly |
---|---|
NC_000011.10:g.96258976T= , CM000673.2:g.96258976T= | GRCh38 |
NC_000011.9:g.95992140T= , CM000673.1:g.95992140T= | GRCh37 |
NC_000011.8:g.95631788T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524717.6:c.513+82407A= MANE Select | ENSP00000434552.1:n.513+82407A= | |
ENST00000524717.5:c.513+82407A= | ENSP00000434552.1:n.513+82407A= | |
NM_032427.3:c.513+82407A= | NP_115803.1:n.513+82407A= | |
XM_011543024.1:c.-172+83932A= | XP_011541326.1:n.-172+83932A= | |
XM_011543025.1:c.513+82407A= | XP_011541327.1:n.513+82407A= | |
XM_011543024.3:c.-172+83932A= | XP_011541326.1:n.-172+83932A= | |
XM_011543025.2:c.513+82407A= | XP_011541327.1:n.513+82407A= | |
NM_032427.4:c.513+82407A= MANE Select | NP_115803.1:n.513+82407A= |