HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940835_67940837del , CM000678.2:g.67940835_67940837del | GRCh38 |
NC_000016.9:g.67974738_67974740del , CM000678.1:g.67974738_67974740del | GRCh37 |
NC_000016.8:g.66532239_66532241del | NCBI36 |
NG_009778.1:g.8277_8279del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.749-358_749-356del MANE Select | ENSP00000264005.5:n.749-358_749-356del | |
ENST00000264005.9:c.749-358_749-356del | ENSP00000264005.5:n.749-358_749-356del | |
ENST00000570369.5:c.156-762_156-760del | ||
ENST00000570980.1:c.533-358_533-356del | ENSP00000464651.1:n.533-358_533-356del | |
ENST00000573538.5:c.392-5_392-3del | ENSP00000463220.1:n.392-5_392-3del | |
NM_000229.1:c.749-358_749-356del | NP_000220.1:n.749-358_749-356del | |
NM_000229.2:c.749-358_749-356del MANE Select | NP_000220.1:n.749-358_749-356del |