HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119422899_119422900del , CM000663.2:g.119422899_119422900del | GRCh38 |
NC_000001.10:g.119965522_119965523del , CM000663.1:g.119965522_119965523del | GRCh37 |
NC_000001.9:g.119767045_119767046del | NCBI36 |
NG_013349.1:g.12969_12970del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369416.4:c.*279_*280del MANE Select | ENSP00000358424.3:n.*279_*280del | |
ENST00000369416.3:c.*279_*280del | ENSP00000358424.3:n.*279_*280del | |
ENST00000543831.5:c.*279_*280del | ENSP00000445122.1:n.*279_*280del | |
NM_000198.3:c.*279_*280del | NP_000189.1:n.*279_*280del | |
NM_001166120.1:c.*279_*280del | NP_001159592.1:n.*279_*280del | |
NM_000198.4:c.*279_*280del MANE Select | NP_000189.1:n.*279_*280del | |
NM_001166120.2:c.*279_*280del | NP_001159592.1:n.*279_*280del |