HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12810784T= , CM000686.2:g.12810784T= | GRCh38 |
NC_000024.9:g.14922719T= , CM000686.1:g.14922719T= | GRCh37 |
NC_000024.8:g.13432113T= | NCBI36 |
NG_008311.1:g.114560T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.4205T= | ENSP00000498372.1:p.Leu1402= | |
ENST00000338981.7:c.4205T= MANE Select | ENSP00000342812.3:p.Leu1402= | |
ENST00000426564.6:n.4217T= | ||
NM_004654.3:c.4205T= | NP_004645.2:p.Leu1402= | |
XM_011531469.1:c.4205T= | XP_011529771.1:p.Leu1402= | |
XM_011531470.1:c.3971T= | XP_011529772.1:p.Leu1324= | |
XM_017030078.2:c.4220T= | XP_016885567.1:p.Leu1407= | |
NM_004654.4:c.4205T= MANE Select | NP_004645.2:p.Leu1402= |