HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114705462del , CM000663.2:g.114705462del | GRCh38 |
NC_000001.10:g.115248083del , CM000663.1:g.115248083del | GRCh37 |
NC_000001.9:g.115049606del | NCBI36 |
NG_007572.1:g.16434del , LRG_92:g.16434del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.*2633del MANE Select | ENSP00000358548.4:n.*2633del | |
ENST00000369535.4:c.*2633del | ENSP00000358548.4:n.*2633del | |
NM_002524.4:c.*2633del | NP_002515.1:n.*2633del | |
NM_002524.5:c.*2633del MANE Select | NP_002515.1:n.*2633del |