HGVS | Genome Assembly |
---|---|
NC_000012.12:g.76346168A>T , CM000674.2:g.76346168A>T | GRCh38 |
NC_000012.11:g.76739948A>T , CM000674.1:g.76739948A>T | GRCh37 |
NC_000012.10:g.75264079A>T | NCBI36 |
NG_016357.1:g.7275T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650064.2:c.1817T>A MANE Select | ENSP00000497413.1:p.Phe606Tyr | |
ENST00000393262.3:c.1817T>A | ENSP00000376946.3:p.Phe606Tyr | |
NM_024685.3:c.1817T>A | NP_078961.3:p.Phe606Tyr | |
NM_024685.4:c.1817T>A MANE Select | NP_078961.3:p.Phe606Tyr |