HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583535del , CM000679.2:g.41583535del | GRCh38 |
NC_000017.10:g.39739787del , CM000679.1:g.39739787del | GRCh37 |
NC_000017.9:g.36993313del | NCBI36 |
NG_008624.1:g.8362del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.1053+17del MANE Select | ENSP00000167586.6:n.1053+17del | |
ENST00000167586.6:c.1053+17del | ENSP00000167586.6:n.1053+17del | |
ENST00000476662.1:n.503+17del | ||
NM_000526.4:c.1053+17del | NP_000517.2:n.1053+17del | |
NM_000526.5:c.1053+17del MANE Select | NP_000517.3:n.1053+17del |