HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872487A>C , CM000673.2:g.124872487A>C | GRCh38 |
NC_000011.9:g.124742383A>C , CM000673.1:g.124742383A>C | GRCh37 |
NC_000011.8:g.124247593A>C | NCBI36 |
NG_016214.1:g.12079A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1265A>C MANE Select | ENSP00000380903.1:p.Tyr422Ser | |
ENST00000397801.5:c.1265A>C | ENSP00000380903.1:p.Tyr422Ser | |
ENST00000538940.5:c.1199A>C | ENSP00000441797.1:p.Tyr400Ser | |
NM_022370.3:c.1265A>C | NP_071765.2:p.Tyr422Ser | |
XM_011542953.1:c.2237A>C | XP_011541255.1:p.Tyr746Ser | |
XM_017018122.1:c.1199A>C | XP_016873611.1:p.Tyr400Ser | |
NM_022370.4:c.1265A>C MANE Select | NP_071765.2:p.Tyr422Ser |