HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34255396C>G , CM000679.2:g.34255396C>G | GRCh38 |
NC_000017.10:g.32582415C>G , CM000679.1:g.32582415C>G | GRCh37 |
NC_000017.9:g.29606528C>G | NCBI36 |
NG_012123.1:g.5120C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000580907.6:c.47C>G | ENSP00000462156.1:p.Thr16Ser | |
ENST00000624362.2:n.112C>G | ||
ENST00000225831.4:c.47C>G MANE Select | ENSP00000225831.4:p.Thr16Ser | |
ENST00000580907.5:c.47C>G | ENSP00000462156.1:p.Thr16Ser | |
ENST00000624362.1:n.179C>G | ||
NM_002982.3:c.47C>G | NP_002973.1:p.Thr16Ser | |
NM_002982.4:c.47C>G MANE Select | NP_002973.1:p.Thr16Ser |