HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101424937T>A , CM000671.2:g.101424937T>A | GRCh38 |
NC_000009.11:g.104187219T>A , CM000671.1:g.104187219T>A | GRCh37 |
NC_000009.10:g.103227040T>A | NCBI36 |
NG_012387.1:g.15844A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.905A>T MANE Select | ENSP00000497767.1:p.Tyr302Phe | |
ENST00000648064.1:c.905A>T | ENSP00000497990.1:p.Tyr302Phe | |
ENST00000648758.1:c.905A>T | ENSP00000497731.1:p.Tyr302Phe | |
ENST00000649902.1:c.905A>T | ENSP00000497216.1:p.Tyr302Phe | |
ENST00000374855.8:c.905A>T | ENSP00000363988.4:p.Tyr302Phe | |
ENST00000616752.1:c.904+1A>T | ENSP00000481363.1:n.904+1A>T | |
NM_000035.3:c.905A>T | NP_000026.2:p.Tyr302Phe | |
NM_000035.4:c.905A>T MANE Select | NP_000026.2:p.Tyr302Phe |