HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138946070C>A , CM000665.2:g.138946070C>A | GRCh38 |
NC_000003.11:g.138664912C>A , CM000665.1:g.138664912C>A | GRCh37 |
NC_000003.10:g.140147602C>A | NCBI36 |
NG_012454.1:g.6071G>T | |
NG_029796.1:g.3837C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.653G>T MANE Select | ENSP00000497217.1:p.Cys218Phe | |
ENST00000330315.3:c.653G>T | ENSP00000333188.3:p.Cys218Phe | |
NM_023067.3:c.653G>T | NP_075555.1:p.Cys218Phe | |
NM_023067.4:c.653G>T MANE Select | NP_075555.1:p.Cys218Phe |