HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882156A>T , CM000663.2:g.160882156A>T | GRCh38 |
NC_000001.10:g.160851946A>T , CM000663.1:g.160851946A>T | GRCh37 |
NC_000001.9:g.159118570A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000326245.4:c.206T>A MANE Select | ENSP00000323587.3:p.Phe69Tyr | |
ENST00000326245.3:c.206T>A | ENSP00000323587.3:p.Phe69Tyr | |
ENST00000464077.1:n.140T>A | ||
NM_017625.2:c.206T>A | NP_060095.2:p.Phe69Tyr | |
NM_017625.3:c.206T>A MANE Select | NP_060095.2:p.Phe69Tyr |