HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169947_110170030del , CM000675.2:g.110169947_110170030del | GRCh38 |
NC_000013.10:g.110822294_110822377del , CM000675.1:g.110822294_110822377del | GRCh37 |
NC_000013.9:g.109620295_109620378del | NCBI36 |
NG_011544.2:g.142121_142204del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375820.10:c.3743-267_3743-184del MANE Select | ENSP00000364979.4:n.3743-267_3743-184del | |
ENST00000375820.8:c.3743-267_3743-184del | ENSP00000364979.4:n.3743-267_3743-184del | |
NM_001845.5:c.3743-267_3743-184del | NP_001836.3:n.3743-267_3743-184del | |
XM_011521048.1:c.3551-267_3551-184del | XP_011519350.1:n.3551-267_3551-184del | |
XM_011521048.2:c.3551-267_3551-184del | XP_011519350.1:n.3551-267_3551-184del | |
NM_001845.6:c.3743-267_3743-184del MANE Select | NP_001836.3:n.3743-267_3743-184del |