HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225468C>A , CM000668.2:g.3225468C>A | GRCh38 |
NC_000006.11:g.3225702C>A , CM000668.1:g.3225702C>A | GRCh37 |
NC_000006.10:g.3170701C>A | NCBI36 |
NG_016715.1:g.7267G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.621G>T MANE Select | ENSP00000259818.6:p.Leu207= | |
ENST00000680070.1:n.1551G>T | ||
ENST00000681707.1:n.1448G>T | ||
ENST00000681757.1:n.926G>T | ||
ENST00000259818.7:c.621G>T | ENSP00000259818.6:p.Leu207= | |
ENST00000473006.1:n.738G>T | ||
NM_178012.4:c.621G>T | NP_821080.1:p.Leu207= | |
XM_011514571.1:c.405G>T | XP_011512873.1:p.Leu135= | |
NM_178012.5:c.621G>T MANE Select | NP_821080.1:p.Leu207= |