HGVS | Genome Assembly |
---|---|
NC_000002.12:g.68653161G>A , CM000664.2:g.68653161G>A | GRCh38 |
NC_000002.11:g.68880293G>A , CM000664.1:g.68880293G>A | GRCh37 |
NC_000002.10:g.68733797G>A | NCBI36 |
NG_051312.1:g.14574G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303786.5:c.486-1719G>A (PROKR1) MANE Select | ENSP00000303775.4:n.486-1719G>A | |
ENST00000303786.4:c.486-1719G>A (PROKR1) | ENSP00000303775.3:n.486-1719G>A | |
ENST00000394342.2:c.486-1719G>A (APLF) | ENSP00000377874.2:n.486-1719G>A | |
ENST00000627740.1:n.1198-1719G>A (APLF) | ||
NM_138964.2:c.486-1719G>A (PROKR1) | NP_620414.1:n.486-1719G>A | |
NM_138964.3:c.486-1719G>A (PROKR1) | NP_620414.1:n.486-1719G>A | |
NM_138964.4:c.486-1719G>A (PROKR1) MANE Select | NP_620414.1:n.486-1719G>A |