HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129818757A>T , CM000671.2:g.129818757A>T | GRCh38 |
NC_000009.11:g.132581036A>T , CM000671.1:g.132581036A>T | GRCh37 |
NC_000009.10:g.131620857A>T | NCBI36 |
NG_008049.1:g.10406T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.608T>A MANE Select | ENSP00000345719.4:p.Phe203Tyr | |
ENST00000651202.1:c.704T>A | ENSP00000498222.1:p.Phe235Tyr | |
ENST00000351698.4:c.608T>A | ENSP00000345719.4:p.Phe203Tyr | |
ENST00000473604.2:n.718T>A | ||
ENST00000474192.1:n.25T>A | ||
NM_000113.2:c.608T>A | NP_000104.1:p.Phe203Tyr | |
XR_929731.1:n.768T>A | ||
XR_929731.3:n.636T>A | ||
NM_000113.3:c.608T>A MANE Select | NP_000104.1:p.Phe203Tyr |