HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400599T= , CM000670.2:g.18400599T= | GRCh38 |
NC_000008.10:g.18258109T= , CM000670.1:g.18258109T= | GRCh37 |
NC_000008.9:g.18302389T= | NCBI36 |
NG_012246.1:g.14355T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.596T= MANE Select | ENSP00000286479.3:p.Ile199= | |
ENST00000286479.3:c.596T= | ENSP00000286479.3:p.Ile199= | |
ENST00000520116.1:c.206T= | ENSP00000428416.1:p.Ile69= | |
NM_000015.2:c.596T= | NP_000006.2:p.Ile199= | |
XM_011544358.1:c.596T= | XP_011542660.1:p.Ile199= | |
XM_017012938.1:c.596T= | XP_016868427.1:p.Ile199= | |
NM_000015.3:c.596T= MANE Select | NP_000006.2:p.Ile199= |