HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12813009A= , CM000686.2:g.12813009A= | GRCh38 |
NC_000024.9:g.14924944A= , CM000686.1:g.14924944A= | GRCh37 |
NC_000024.8:g.13434338A= | NCBI36 |
NG_008311.1:g.116785A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.4566A= | ENSP00000498372.1:p.Val1522= | |
ENST00000338981.7:c.4566A= MANE Select | ENSP00000342812.3:p.Val1522= | |
ENST00000426564.6:n.4578A= | ||
NM_004654.3:c.4566A= | NP_004645.2:p.Val1522= | |
XM_011531469.1:c.4566A= | XP_011529771.1:p.Val1522= | |
XM_011531470.1:c.4332A= | XP_011529772.1:p.Val1444= | |
XM_017030078.2:c.4581A= | XP_016885567.1:p.Val1527= | |
NM_004654.4:c.4566A= MANE Select | NP_004645.2:p.Val1522= |