HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431988del , CM000663.2:g.229431988del | GRCh38 |
NC_000001.10:g.229567735del , CM000663.1:g.229567735del | GRCh37 |
NC_000001.9:g.227634358del | NCBI36 |
NG_006672.1:g.7112del , LRG_429:g.7112del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366683.4:c.808+9del | ENSP00000355644.4:n.808+9del | |
ENST00000684723.1:c.673+9del | ENSP00000508084.1:n.673+9del | |
ENST00000366683.3:c.480-123del | ENSP00000355644.3:n.480-123del | |
ENST00000366684.7:c.808+9del MANE Select | ENSP00000355645.3:n.808+9del | |
NM_001100.3:c.808+9del , LRG_429t1:c.808+9del | NP_001091.1:n.808+9del | |
NM_001100.4:c.808+9del MANE Select | NP_001091.1:n.808+9del |