HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12778053C= , CM000686.2:g.12778053C= | GRCh38 |
NC_000024.9:g.14889987C= , CM000686.1:g.14889987C= | GRCh37 |
NC_000024.8:g.13399381C= | NCBI36 |
NG_008311.1:g.81828C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.2674C= | ENSP00000498372.1:p.Arg892= | |
ENST00000338981.7:c.2674C= MANE Select | ENSP00000342812.3:p.Arg892= | |
ENST00000426564.6:n.2686C= | ||
NM_004654.3:c.2674C= | NP_004645.2:p.Arg892= | |
XM_011531469.1:c.2674C= | XP_011529771.1:p.Arg892= | |
XM_011531470.1:c.2440C= | XP_011529772.1:p.Arg814= | |
XM_017030078.2:c.2689C= | XP_016885567.1:p.Arg897= | |
NM_004654.4:c.2674C= MANE Select | NP_004645.2:p.Arg892= |