HGVS | Genome Assembly |
---|---|
NC_000023.11:g.83508941T>A , CM000685.2:g.83508941T>A | GRCh38 |
NC_000023.10:g.82763949T>A , CM000685.1:g.82763949T>A | GRCh37 |
NC_000023.9:g.82650605T>A | NCBI36 |
NG_009936.2:g.5681T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644024.2:c.617T>A MANE Select | ENSP00000495996.1:p.Ile206Asn | |
ENST00000373200.4:c.617T>A | ENSP00000362296.2:p.Ile206Asn | |
NM_000307.4:c.617T>A | NP_000298.3:p.Ile206Asn | |
NM_000307.5:c.617T>A MANE Select | NP_000298.3:p.Ile206Asn |