HGVS | Genome Assembly |
---|---|
NC_000020.11:g.2394427_2394437del , CM000682.2:g.2394427_2394437del | GRCh38 |
NC_000020.10:g.2375073_2375083del , CM000682.1:g.2375073_2375083del | GRCh37 |
NC_000020.9:g.2323073_2323083del | NCBI36 |
NG_031917.1:g.18520_18530del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000202625.7:c.8-25_8-15del MANE Select | ENSP00000202625.2:n.8-25_8-15del | |
ENST00000202625.6:c.8-25_8-15del | ENSP00000202625.2:n.8-25_8-15del | |
ENST00000381423.1:c.8-25_8-15del | ENSP00000370831.1:n.8-25_8-15del | |
NM_001254734.1:c.8-25_8-15del | NP_001241663.1:n.8-25_8-15del | |
NM_198994.2:c.8-25_8-15del | NP_945345.2:n.8-25_8-15del | |
NM_001254734.2:c.8-25_8-15del | NP_001241663.1:n.8-25_8-15del | |
NM_198994.3:c.8-25_8-15del MANE Select | NP_945345.2:n.8-25_8-15del |