HGVS | Genome Assembly |
---|---|
NC_000023.11:g.83508604A>T , CM000685.2:g.83508604A>T | GRCh38 |
NC_000023.10:g.82763612A>T , CM000685.1:g.82763612A>T | GRCh37 |
NC_000023.9:g.82650268A>T | NCBI36 |
NG_009936.2:g.5344A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644024.2:c.280A>T MANE Select | ENSP00000495996.1:p.Ile94Phe | |
ENST00000373200.4:c.280A>T | ENSP00000362296.2:p.Ile94Phe | |
NM_000307.4:c.280A>T | NP_000298.3:p.Ile94Phe | |
NM_000307.5:c.280A>T MANE Select | NP_000298.3:p.Ile94Phe |