HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10612914A>T , CM000670.2:g.10612914A>T | GRCh38 |
NC_000008.10:g.10470424A>T , CM000670.1:g.10470424A>T | GRCh37 |
NC_000008.9:g.10507834A>T | NCBI36 |
NG_028035.1:g.47194T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.1184T>A MANE Select | ENSP00000371923.3:p.Phe395Tyr | |
ENST00000382483.3:c.1184T>A | ENSP00000371923.3:p.Phe395Tyr | |
NM_178857.5:c.1184T>A | NP_849188.4:p.Phe395Tyr | |
NM_178857.6:c.1184T>A MANE Select | NP_849188.4:p.Phe395Tyr |