HGVS | Genome Assembly |
---|---|
NC_000019.10:g.12800391C>A , CM000681.2:g.12800391C>A | GRCh38 |
NC_000019.9:g.12911205C>A , CM000681.1:g.12911205C>A | GRCh37 |
NC_000019.8:g.12772205C>A | NCBI36 |
NG_029901.1:g.6490G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301522.3:c.258-92G>T (PRDX2) MANE Select | ENSP00000301522.2:n.258-92G>T | |
ENST00000301522.2:c.258-92G>T (PRDX2) | ENSP00000301522.2:n.258-92G>T | |
ENST00000334482.9:c.258-92G>T (PRDX2) | ENSP00000334063.5:n.258-92G>T | |
ENST00000466174.5:n.841G>T (PRDX2) | ||
ENST00000477555.1:n.316-92G>T (PRDX2) | ||
ENST00000478908.1:n.71G>T (PRDX2) | ||
ENST00000589765.1:n.41+24787G>T (HOOK2) | ||
NM_005809.5:c.258-92G>T (PRDX2) | NP_005800.3:n.258-92G>T | |
NM_005809.6:c.258-92G>T (PRDX2) MANE Select | NP_005800.3:n.258-92G>T |