HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586677_41586681delinsGAGAC , CM000679.2:g.41586677_41586681delinsGAGAC | GRCh38 |
NC_000017.10:g.39742929_39742933delinsGAGAC , CM000679.1:g.39742929_39742933delinsGAGAC | GRCh37 |
NC_000017.9:g.36996455_36996459delinsGAGAC | NCBI36 |
NG_008624.1:g.5215_5219delinsGTCTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.154_158delinsGTCTC MANE Select | ENSP00000167586.6:p.Val52= | |
ENST00000167586.6:c.154_158delinsGTCTC | ENSP00000167586.6:p.Val52= | |
NM_000526.4:c.154_158delinsGTCTC | NP_000517.2:p.Val52= | |
NM_000526.5:c.154_158delinsGTCTC MANE Select | NP_000517.3:p.Val52= |