HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176719_21176729dup , CM000674.2:g.21176719_21176729dup | GRCh38 |
NC_000012.11:g.21329653_21329663dup , CM000674.1:g.21329653_21329663dup | GRCh37 |
NC_000012.10:g.21220920_21220930dup | NCBI36 |
NG_011745.1:g.50526_50536dup , LRG_1022:g.50526_50536dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.360-57_360-47dup MANE Select | ENSP00000256958.2:n.360-57_360-47dup | |
ENST00000256958.2:c.360-57_360-47dup | ENSP00000256958.2:n.360-57_360-47dup | |
ENST00000543498.5:c.426-57_426-47dup | ||
NM_006446.4:c.360-57_360-47dup , LRG_1022t1:c.360-57_360-47dup | NP_006437.3:n.360-57_360-47dup | |
NM_006446.5:c.360-57_360-47dup MANE Select | NP_006437.3:n.360-57_360-47dup |