HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153737199T>G , CM000685.2:g.153737199T>G | GRCh38 |
NC_000023.10:g.153002653T>G , CM000685.1:g.153002653T>G | GRCh37 |
NC_000023.9:g.152655847T>G | NCBI36 |
NG_009022.2:g.17332T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1436T>G MANE Select | ENSP00000218104.3:p.Ile479Ser | |
ENST00000218104.5:c.1436T>G | ENSP00000218104.3:p.Ile479Ser | |
ENST00000443684.2:n.439T>G | ||
NM_000033.3:c.1436T>G | NP_000024.2:p.Ile479Ser | |
XR_938507.1:n.1908T>G | ||
XR_938507.2:n.1908T>G | ||
NM_000033.4:c.1436T>G MANE Select | NP_000024.2:p.Ile479Ser |