HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18388589_18388603del , CM000681.2:g.18388589_18388603del | GRCh38 |
NC_000019.9:g.18499399_18499413del , CM000681.1:g.18499399_18499413del | GRCh37 |
NC_000019.8:g.18360399_18360413del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000595973.3:c.581_595del | ENSP00000470531.3:p.Arg194_Arg198del | |
ENST00000597765.2:c.581_595del | ENSP00000469819.2:p.Arg194_Arg198del | |
ENST00000252809.3:c.581_595del MANE Select | ENSP00000252809.3:p.Arg194_Arg198del | |
NM_004864.2:c.581_595del | NP_004855.2:p.Arg194_Arg198del | |
NM_004864.3:c.581_595del | NP_004855.2:p.Arg194_Arg198del | |
XM_024451789.1:c.581_595del | XP_024307557.1:p.Arg194_Arg198del | |
NM_004864.4:c.581_595del MANE Select | NP_004855.2:p.Arg194_Arg198del |