HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140333236_140333237insT , CM000667.2:g.140333236_140333237insT | GRCh38 |
NC_000005.9:g.139712821_139712822insT , CM000667.1:g.139712821_139712822insT | GRCh37 |
NC_000005.8:g.139693005_139693006insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000230990.7:c.*1062_*1063insA MANE Select | ENSP00000230990.6:n.*1062_*1063insA | |
ENST00000230990.6:c.*1062_*1063insA | ENSP00000230990.6:n.*1062_*1063insA | |
NM_001945.2:c.*1062_*1063insA | NP_001936.1:n.*1062_*1063insA | |
NM_001945.3:c.*1062_*1063insA MANE Select | NP_001936.1:n.*1062_*1063insA |