HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371589A>T , CM000680.2:g.60371589A>T | GRCh38 |
NC_000018.9:g.58038822A>T , CM000680.1:g.58038822A>T | GRCh37 |
NC_000018.8:g.56189802A>T | NCBI36 |
NG_016441.1:g.6180T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.761T>A MANE Select | ENSP00000299766.3:p.Phe254Tyr | |
ENST00000299766.4:c.761T>A | ENSP00000299766.3:p.Phe254Tyr | |
NM_005912.2:c.761T>A | NP_005903.2:p.Phe254Tyr | |
NM_005912.3:c.761T>A MANE Select | NP_005903.2:p.Phe254Tyr |