HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713911_114713913del , CM000663.2:g.114713911_114713913del | GRCh38 |
NC_000001.10:g.115256532_115256534del , CM000663.1:g.115256532_115256534del | GRCh37 |
NC_000001.9:g.115058055_115058057del | NCBI36 |
NG_007572.1:g.7982_7984del , LRG_92:g.7982_7984del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.177_179del MANE Select | ENSP00000358548.4:p.Gly60del | |
ENST00000369535.4:c.177_179del | ENSP00000358548.4:p.Gly60del | |
NM_002524.4:c.177_179del | NP_002515.1:p.Gly60del | |
NM_002524.5:c.177_179del MANE Select | NP_002515.1:p.Gly60del |