HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138946061_138946063del , CM000665.2:g.138946061_138946063del | GRCh38 |
NC_000003.11:g.138664903_138664905del , CM000665.1:g.138664903_138664905del | GRCh37 |
NC_000003.10:g.140147593_140147595del | NCBI36 |
NG_012454.1:g.6081_6083del | |
NG_029796.1:g.3828_3830del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.663_665del MANE Select | ENSP00000497217.1:p.Ala222del | |
ENST00000330315.3:c.663_665del | ENSP00000333188.3:p.Ala222del | |
NM_023067.3:c.663_665del | NP_075555.1:p.Ala222del | |
NM_023067.4:c.663_665del MANE Select | NP_075555.1:p.Ala222del |