HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583728_41583735del , CM000679.2:g.41583728_41583735del | GRCh38 |
NC_000017.10:g.39739980_39739987del , CM000679.1:g.39739980_39739987del | GRCh37 |
NC_000017.9:g.36993506_36993513del | NCBI36 |
NG_008624.1:g.8161_8168del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.927+25_927+32del MANE Select | ENSP00000167586.6:n.927+25_927+32del | |
ENST00000167586.6:c.927+25_927+32del | ENSP00000167586.6:n.927+25_927+32del | |
ENST00000476662.1:n.377+25_377+32del | ||
NM_000526.4:c.927+25_927+32del | NP_000517.2:n.927+25_927+32del | |
NM_000526.5:c.927+25_927+32del MANE Select | NP_000517.3:n.927+25_927+32del |