HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598664C>G , CM000680.2:g.31598664C>G | GRCh38 |
NC_000018.9:g.29178627C>G , CM000680.1:g.29178627C>G | GRCh37 |
NC_000018.8:g.27432625C>G | NCBI36 |
NG_009490.1:g.11898C>G , LRG_416:g.11898C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000237014.8:c.433C>G MANE Select | ENSP00000237014.4:p.Pro145Ala | |
ENST00000610404.5:c.337C>G | ENSP00000477599.2:p.Pro113Ala | |
ENST00000649620.1:c.433C>G | ENSP00000497927.1:p.Pro145Ala | |
ENST00000237014.7:c.433C>G | ENSP00000237014.3:p.Pro145Ala | |
ENST00000610404.4:c.547C>G | ENSP00000477599.1:p.Pro183Ala | |
ENST00000613781.1:c.409C>G | ENSP00000479174.1:p.Pro137Ala | |
NM_000371.3:c.433C>G , LRG_416t1:c.433C>G | NP_000362.1:p.Pro145Ala | |
NM_000371.4:c.433C>G MANE Select | NP_000362.1:p.Pro145Ala |