HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013161_25013190del , CM000685.2:g.25013161_25013190del | GRCh38 |
NC_000023.10:g.25031278_25031307del , CM000685.1:g.25031278_25031307del | GRCh37 |
NC_000023.9:g.24941199_24941228del | NCBI36 |
NG_008281.1:g.7764_7793del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.810_839del MANE Select | ENSP00000368332.4:p.Thr271_Ala280del | |
ENST00000379044.4:c.810_839del | ENSP00000368332.4:p.Thr271_Ala280del | |
NM_139058.2:c.810_839del | NP_620689.1:p.Thr271_Ala280del | |
NM_139058.3:c.810_839del MANE Select | NP_620689.1:p.Thr271_Ala280del |