HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215728428_215728429del , CM000663.2:g.215728428_215728429del | GRCh38 |
NC_000001.10:g.215901770_215901771del , CM000663.1:g.215901770_215901771del | GRCh37 |
NC_000001.9:g.213968393_213968394del | NCBI36 |
NG_009497.1:g.699968_699969del | |
NG_009497.2:g.700020_700021del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11712-45_11712-44del MANE Select | ENSP00000305941.3:n.11712-45_11712-44del | |
ENST00000674083.1:c.11712-45_11712-44del | ENSP00000501296.1:n.11712-45_11712-44del | |
ENST00000307340.7:c.11712-45_11712-44del | ENSP00000305941.3:n.11712-45_11712-44del | |
NM_206933.2:c.11712-45_11712-44del | NP_996816.2:n.11712-45_11712-44del | |
NM_206933.3:c.11712-45_11712-44del | NP_996816.2:n.11712-45_11712-44del | |
NM_206933.4:c.11712-45_11712-44del MANE Select | NP_996816.3:n.11712-45_11712-44del |