HGVS | Genome Assembly |
---|---|
NC_000019.10:g.12800397T>C , CM000681.2:g.12800397T>C | GRCh38 |
NC_000019.9:g.12911211T>C , CM000681.1:g.12911211T>C | GRCh37 |
NC_000019.8:g.12772211T>C | NCBI36 |
NG_029901.1:g.6484A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301522.3:c.258-98A>G (PRDX2) MANE Select | ENSP00000301522.2:n.258-98A>G | |
ENST00000301522.2:c.258-98A>G (PRDX2) | ENSP00000301522.2:n.258-98A>G | |
ENST00000334482.9:c.258-98A>G (PRDX2) | ENSP00000334063.5:n.258-98A>G | |
ENST00000466174.5:n.835A>G (PRDX2) | ||
ENST00000477555.1:n.316-98A>G (PRDX2) | ||
ENST00000478908.1:n.65A>G (PRDX2) | ||
ENST00000589765.1:n.41+24781A>G (HOOK2) | ||
NM_005809.5:c.258-98A>G (PRDX2) | NP_005800.3:n.258-98A>G | |
NM_005809.6:c.258-98A>G (PRDX2) MANE Select | NP_005800.3:n.258-98A>G |