HGVS | Genome Assembly |
---|---|
NC_000018.10:g.59269154_59269216del , CM000680.2:g.59269154_59269216del | GRCh38 |
NC_000018.9:g.56936386_56936448del , CM000680.1:g.56936386_56936448del | GRCh37 |
NC_000018.8:g.55087366_55087428del | NCBI36 |
NG_013031.1:g.9189_9251del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000334889.4:c.840_902del MANE Select | ENSP00000334813.3:p.Pro281_Pro301del | |
ENST00000256852.7:c.*271_*333del | ENSP00000256852.7:n.*271_*333del | |
ENST00000334889.3:c.840_902del | ENSP00000334813.3:p.Pro281_Pro301del | |
NM_013435.2:c.840_902del | NP_038463.2:p.Pro281_Pro301del | |
NM_013435.3:c.840_902del MANE Select | NP_038463.2:p.Pro281_Pro301del |