HGVS | Genome Assembly |
---|---|
NC_000015.10:g.67066055del , CM000677.2:g.67066055del | GRCh38 |
NC_000015.9:g.67358393del , CM000677.1:g.67358393del | GRCh37 |
NC_000015.8:g.65145447del | NCBI36 |
NG_011990.1:g.5199del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559460.6:c.-110+2111del | ENSP00000453082.2:n.-110+2111del | |
ENST00000560424.2:c.-100del | ENSP00000455540.2:n.-100del | |
ENST00000327367.9:c.-100del MANE Select | ENSP00000332973.4:n.-100del | |
ENST00000327367.8:c.-100del | ENSP00000332973.4:n.-100del | |
ENST00000559460.5:c.-110+2111del | ENSP00000453082.1:n.-110+2111del | |
NM_005902.3:c.-100del | NP_005893.1:n.-100del | |
XM_011521559.1:c.-100del | XP_011519861.1:n.-100del | |
NM_005902.4:c.-100del MANE Select | NP_005893.1:n.-100del |