HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94001830C= , CM000663.2:g.94001830C= | GRCh38 |
NC_000001.10:g.94467386C= , CM000663.1:g.94467386C= | GRCh37 |
NC_000001.9:g.94239974C= | NCBI36 |
NG_009073.1:g.124320G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.6282+28G= MANE Select | ENSP00000359245.3:n.6282+28G= | |
ENST00000370225.3:c.6282+28G= | ENSP00000359245.3:n.6282+28G= | |
ENST00000465352.1:n.726G= | ||
ENST00000536513.5:c.2658+28G= | ENSP00000439707.2:n.2658+28G= | |
NM_000350.2:c.6282+28G= | NP_000341.2:n.6282+28G= | |
NM_000350.3:c.6282+28G= MANE Select | NP_000341.2:n.6282+28G= |