HGVS | Genome Assembly |
---|---|
NC_000023.11:g.9741395G>C , CM000685.2:g.9741395G>C | GRCh38 |
NC_000023.10:g.9709435G>C , CM000685.1:g.9709435G>C | GRCh37 |
NC_000023.9:g.9669435G>C | NCBI36 |
NG_009074.1:g.29483C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467482.6:c.828C>G MANE Select | ENSP00000417161.1:p.Ile276Met | |
ENST00000447366.5:c.576C>G | ENSP00000390546.2:p.Ile192Met | |
ENST00000467482.5:c.828C>G | ENSP00000417161.1:p.Ile276Met | |
NM_000273.2:c.828C>G | NP_000264.2:p.Ile276Met | |
XM_005274541.2:c.828C>G | XP_005274598.1:p.Ile276Met | |
XM_005274541.3:c.828C>G | XP_005274598.1:p.Ile276Met | |
XM_024452387.1:c.576C>G | XP_024308155.1:p.Ile192Met | |
XM_024452388.1:c.576C>G | XP_024308156.1:p.Ile192Met | |
NM_000273.3:c.828C>G MANE Select | NP_000264.2:p.Ile276Met |