HGVS | Genome Assembly |
---|---|
NC_000007.14:g.27095694_27095696del , CM000669.2:g.27095694_27095696del | GRCh38 |
NC_000007.13:g.27135313_27135315del , CM000669.1:g.27135313_27135315del | GRCh37 |
NC_000007.12:g.27101838_27101840del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643460.2:c.218_220del MANE Select | ENSP00000494260.2:p.Arg73del | |
ENST00000343060.4:c.218_220del | ENSP00000343246.4:p.Arg73del | |
ENST00000355633.5:c.218_220del | ENSP00000347851.5:p.Arg73del | |
NM_005522.5:c.218_220del MANE Select | NP_005513.2:p.Arg73del | |
NM_153620.3:c.218_220del | NP_705873.3:p.Arg73del |