HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204159301_204159310del , CM000663.2:g.204159301_204159310del | GRCh38 |
NC_000001.10:g.204128429_204128438del , CM000663.1:g.204128429_204128438del | GRCh37 |
NC_000001.9:g.202395052_202395061del | NCBI36 |
NG_012122.1:g.12030_12039del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272190.9:c.689+91_689+100del MANE Select | ENSP00000272190.8:n.689+91_689+100del | |
ENST00000638118.1:c.575+91_575+100del | ENSP00000490307.1:n.575+91_575+100del | |
ENST00000272190.8:c.689+91_689+100del | ENSP00000272190.8:n.689+91_689+100del | |
NM_000537.3:c.689+91_689+100del | NP_000528.1:n.689+91_689+100del | |
NM_000537.4:c.689+91_689+100del MANE Select | NP_000528.1:n.689+91_689+100del |