HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011157T>A , CM000682.2:g.46011157T>A | GRCh38 |
NC_000020.10:g.44639796T>A , CM000682.1:g.44639796T>A | GRCh37 |
NC_000020.9:g.44073203T>A | NCBI36 |
NG_011468.1:g.7250T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.664T>A MANE Select | ENSP00000361405.3:p.Phe222Ile | |
NM_004994.2:c.664T>A | NP_004985.2:p.Phe222Ile | |
NM_004994.3:c.664T>A MANE Select | NP_004985.2:p.Phe222Ile |