HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43887153_43887164del , CM000664.2:g.43887153_43887164del | GRCh38 |
NC_000002.11:g.44114292_44114303del , CM000664.1:g.44114292_44114303del | GRCh37 |
NC_000002.10:g.43967796_43967807del | NCBI36 |
NG_008247.1:g.113851_113862del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2397_2408del | ||
ENST00000684454.1:n.9494_9505del | ||
ENST00000260665.12:c.*1445_*1456del MANE Select | ENSP00000260665.7:n.*1445_*1456del | |
ENST00000260665.11:c.*1445_*1456del | ENSP00000260665.7:n.*1445_*1456del | |
NM_133259.3:c.*1445_*1456del | NP_573566.2:n.*1445_*1456del | |
XR_002958896.1:n.5812_5823del | ||
NM_133259.4:c.*1445_*1456del MANE Select | NP_573566.2:n.*1445_*1456del |