HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675647_215675648del , CM000663.2:g.215675647_215675648del | GRCh38 |
NC_000001.10:g.215848989_215848990del , CM000663.1:g.215848989_215848990del | GRCh37 |
NC_000001.9:g.213915612_213915613del | NCBI36 |
NG_009497.1:g.752749_752750del | |
NG_009497.2:g.752801_752802del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12295-32_12295-31del MANE Select | ENSP00000305941.3:n.12295-32_12295-31del | |
ENST00000674083.1:c.12295-32_12295-31del | ENSP00000501296.1:n.12295-32_12295-31del | |
ENST00000307340.7:c.12295-32_12295-31del | ENSP00000305941.3:n.12295-32_12295-31del | |
NM_206933.2:c.12295-32_12295-31del | NP_996816.2:n.12295-32_12295-31del | |
NM_206933.3:c.12295-32_12295-31del | NP_996816.2:n.12295-32_12295-31del | |
NM_206933.4:c.12295-32_12295-31del MANE Select | NP_996816.3:n.12295-32_12295-31del |