HGVS | Genome Assembly |
---|---|
NC_000017.11:g.73196414_73196415del , CM000679.2:g.73196414_73196415del | GRCh38 |
NC_000017.10:g.71192553_71192554del , CM000679.1:g.71192553_71192554del | GRCh37 |
NC_000017.9:g.68704148_68704149del | NCBI36 |
NG_008971.1:g.8381_8382del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299886.9:c.316-93_316-92del MANE Select | ENSP00000299886.4:n.316-93_316-92del | |
ENST00000299886.8:c.316-93_316-92del | ENSP00000299886.4:n.316-93_316-92del | |
ENST00000438720.7:c.314-93_314-92del | ||
ENST00000582587.2:c.293-73_293-72del | ||
ENST00000618996.4:c.316-93_316-92del | ENSP00000479450.1:n.316-93_316-92del | |
NM_018714.2:c.316-93_316-92del | NP_061184.1:n.316-93_316-92del | |
NM_018714.3:c.316-93_316-92del MANE Select | NP_061184.1:n.316-93_316-92del |