HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586333T>G , CM000679.2:g.41586333T>G | GRCh38 |
NC_000017.10:g.39742585T>G , CM000679.1:g.39742585T>G | GRCh37 |
NC_000017.9:g.36996111T>G | NCBI36 |
NG_008624.1:g.5563A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.502A>C MANE Select | ENSP00000167586.6:p.Thr168Pro | |
ENST00000167586.6:c.502A>C | ENSP00000167586.6:p.Thr168Pro | |
NM_000526.4:c.502A>C | NP_000517.2:p.Thr168Pro | |
NM_000526.5:c.502A>C MANE Select | NP_000517.3:p.Thr168Pro |