HGVS | Genome Assembly |
---|---|
NC_000011.10:g.92971947A= , CM000673.2:g.92971947A= | GRCh38 |
NC_000011.9:g.92705113A= , CM000673.1:g.92705113A= | GRCh37 |
NC_000011.8:g.92344761A= | NCBI36 |
NG_028160.1:g.7325A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257068.3:c.223+1999A= MANE Select | ENSP00000257068.2:n.223+1999A= | |
ENST00000257068.2:c.223+1999A= | ENSP00000257068.2:n.223+1999A= | |
ENST00000528076.1:c.165+1999A= | ||
ENST00000532482.1:c.224-514A= | ENSP00000436101.1:n.224-514A= | |
NM_005959.3:c.223+1999A= | NP_005950.1:n.223+1999A= | |
XM_011542839.1:c.223+1999A= | XP_011541141.1:n.223+1999A= | |
XM_011542839.2:c.223+1999A= | XP_011541141.1:n.223+1999A= | |
NM_005959.5:c.223+1999A= MANE Select | NP_005950.1:n.223+1999A= |