HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32220464_32220478del , CM000668.2:g.32220464_32220478del | GRCh38 |
NC_000006.11:g.32188241_32188255del , CM000668.1:g.32188241_32188255del | GRCh37 |
NC_000006.10:g.32296219_32296233del | NCBI36 |
NG_028190.1:g.8590_8604del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.1086_1100del MANE Select | ENSP00000364163.3:p.Thr363_Gly367del | |
ENST00000473562.1:n.1215_1229del | ||
NM_004557.3:c.1086_1100del | NP_004548.3:p.Thr363_Gly367del | |
NR_134949.1:n.1225_1239del | ||
NR_134950.1:n.1225_1239del | ||
NM_004557.4:c.1086_1100del MANE Select | NP_004548.3:p.Thr363_Gly367del | |
NR_134949.2:n.1225_1239del | ||
NR_134950.2:n.1225_1239del |