HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940831_67940834del , CM000678.2:g.67940831_67940834del | GRCh38 |
NC_000016.9:g.67974734_67974737del , CM000678.1:g.67974734_67974737del | GRCh37 |
NC_000016.8:g.66532235_66532238del | NCBI36 |
NG_009778.1:g.8279_8282del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.749-356_749-353del MANE Select | ENSP00000264005.5:n.749-356_749-353del | |
ENST00000264005.9:c.749-356_749-353del | ENSP00000264005.5:n.749-356_749-353del | |
ENST00000570369.5:c.156-760_156-757del | ||
ENST00000570980.1:c.533-356_533-353del | ENSP00000464651.1:n.533-356_533-353del | |
ENST00000573538.5:c.392-3_392del | ||
NM_000229.1:c.749-356_749-353del | NP_000220.1:n.749-356_749-353del | |
NM_000229.2:c.749-356_749-353del MANE Select | NP_000220.1:n.749-356_749-353del |