HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215728444_215728451del , CM000663.2:g.215728444_215728451del | GRCh38 |
NC_000001.10:g.215901786_215901793del , CM000663.1:g.215901786_215901793del | GRCh37 |
NC_000001.9:g.213968409_213968416del | NCBI36 |
NG_009497.1:g.699946_699953del | |
NG_009497.2:g.699998_700005del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11712-67_11712-60del MANE Select | ENSP00000305941.3:n.11712-67_11712-60del | |
ENST00000674083.1:c.11712-67_11712-60del | ENSP00000501296.1:n.11712-67_11712-60del | |
ENST00000307340.7:c.11712-67_11712-60del | ENSP00000305941.3:n.11712-67_11712-60del | |
NM_206933.2:c.11712-67_11712-60del | NP_996816.2:n.11712-67_11712-60del | |
NM_206933.3:c.11712-67_11712-60del | NP_996816.2:n.11712-67_11712-60del | |
NM_206933.4:c.11712-67_11712-60del MANE Select | NP_996816.3:n.11712-67_11712-60del |