HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586386C>G , CM000679.2:g.41586386C>G | GRCh38 |
NC_000017.10:g.39742638C>G , CM000679.1:g.39742638C>G | GRCh37 |
NC_000017.9:g.36996164C>G | NCBI36 |
NG_008624.1:g.5510G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.449G>C MANE Select | ENSP00000167586.6:p.Trp150Ser | |
ENST00000167586.6:c.449G>C | ENSP00000167586.6:p.Trp150Ser | |
NM_000526.4:c.449G>C | NP_000517.2:p.Trp150Ser | |
NM_000526.5:c.449G>C MANE Select | NP_000517.3:p.Trp150Ser |