HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645563T>G , CM000663.2:g.20645563T>G | GRCh38 |
NC_000001.10:g.20972056T>G , CM000663.1:g.20972056T>G | GRCh37 |
NC_000001.9:g.20844643T>G | NCBI36 |
NG_008164.1:g.17109T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321556.5:c.963T>G (PINK1) MANE Select | ENSP00000364204.3:p.Tyr321Ter | |
ENST00000321556.4:c.963T>G (PINK1) | ENSP00000364204.3:p.Tyr321Ter | |
ENST00000400490.2:n.56T>G (PINK1) | ||
ENST00000492302.1:n.2051T>G (PINK1) | ||
NM_032409.2:c.963T>G (PINK1) | NP_115785.1:p.Tyr321Ter | |
NR_046507.1:n.3981+22A>C (PINK1-AS) | ||
NM_032409.3:c.963T>G (PINK1) MANE Select | NP_115785.1:p.Tyr321Ter |