HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145127_38145131del , CM000670.2:g.38145127_38145131del | GRCh38 |
NC_000008.10:g.38002645_38002649del , CM000670.1:g.38002645_38002649del | GRCh37 |
NC_000008.9:g.38121802_38121806del | NCBI36 |
NG_011827.1:g.10956_10960del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.744+95_744+99del MANE Select | ENSP00000276449.3:n.744+95_744+99del | |
ENST00000276449.8:c.744+95_744+99del | ENSP00000276449.3:n.744+95_744+99del | |
ENST00000520114.1:n.1973_1977del | ||
ENST00000522050.1:c.587-741_587-737del | ||
NM_000349.2:c.744+95_744+99del | NP_000340.2:n.744+95_744+99del | |
XM_006716392.1:c.651-741_651-737del | XP_006716455.1:n.651-741_651-737del | |
NM_000349.3:c.744+95_744+99del MANE Select | NP_000340.2:n.744+95_744+99del |