HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32814372G= , CM000668.2:g.32814372G= | GRCh38 |
NC_000006.11:g.32782149G= , CM000668.1:g.32782149G= | GRCh37 |
NC_000006.10:g.32890127G= | NCBI36 |
NG_009793.3:g.29399C= | |
NG_012008.1:g.7677C= | |
NG_009793.4:g.29399C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000438763.7:c.591C= MANE Select | ENSP00000390020.2:p.Tyr197= | |
ENST00000648009.1:c.591C= | ENSP00000496848.1:p.Tyr197= | |
ENST00000438763.6:c.591C= | ENSP00000390020.2:p.Tyr197= | |
ENST00000447394.1:c.541C= | ||
ENST00000452392.2:c.2412C= | ENSP00000391806.2:p.Tyr804= | |
ENST00000475235.1:n.628C= | ||
ENST00000488325.5:c.*362C= | ENSP00000436618.1:n.*362C= | |
NM_002120.3:c.591C= | NP_002111.1:p.Tyr197= | |
NM_002120.4:c.591C= MANE Select | NP_002111.1:p.Tyr197= |