HGVS | Genome Assembly |
---|---|
NC_000005.10:g.146339887dup , CM000667.2:g.146339887dup | GRCh38 |
NC_000005.9:g.145719450dup , CM000667.1:g.145719450dup | GRCh37 |
NC_000005.8:g.145699643dup | NCBI36 |
NG_011885.1:g.5864dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000646991.2:c.460dup MANE Select | ENSP00000495718.1:p.His154ProfsTer18 | |
ENST00000230732.4:c.460dup | ENSP00000230732.4:p.His154ProfsTer18 | |
NM_002700.2:c.460dup | NP_002691.1:p.His154ProfsTer18 | |
NM_002700.3:c.460dup MANE Select | NP_002691.1:p.His154ProfsTer18 |