HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951844A>G , CM000670.2:g.19951844A>G | GRCh38 |
NC_000008.10:g.19809355A>G , CM000670.1:g.19809355A>G | GRCh37 |
NC_000008.9:g.19853635A>G | NCBI36 |
NG_008855.1:g.17774A>G | |
NG_008855.2:g.55128A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.325A>G MANE Select | ENSP00000497642.1:p.Ile109Val | |
ENST00000311322.8:c.325A>G | ENSP00000309757.6:p.Ile109Val | |
ENST00000520959.5:c.97A>G | ENSP00000428496.1:p.Ile33Val | |
ENST00000524029.5:c.325A>G | ENSP00000428237.1:p.Ile109Val | |
NM_000237.2:c.325A>G | NP_000228.1:p.Ile109Val | |
NM_000237.3:c.325A>G MANE Select | NP_000228.1:p.Ile109Val |