HGVS | Genome Assembly |
---|---|
NC_000002.12:g.206122267_206122268del , CM000664.2:g.206122267_206122268del | GRCh38 |
NC_000002.11:g.206986991_206986992del , CM000664.1:g.206986991_206986992del | GRCh37 |
NC_000002.10:g.206695236_206695237del | NCBI36 |
NG_009248.1:g.42197_42198del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233190.11:c.*1918_*1919del MANE Select | ENSP00000233190.5:n.*1918_*1919del | |
ENST00000233190.10:c.*1918_*1919del | ENSP00000233190.5:n.*1918_*1919del | |
NM_001199981.2:c.*1918_*1919del | NP_001186910.1:n.*1918_*1919del | |
NM_001199982.2:c.*1918_*1919del | NP_001186911.1:n.*1918_*1919del | |
NM_001199983.2:c.*1918_*1919del | NP_001186912.1:n.*1918_*1919del | |
NM_005006.7:c.*1918_*1919del MANE Select | NP_004997.4:n.*1918_*1919del | |
NM_001199984.2:c.*1918_*1919del | NP_001186913.1:n.*1918_*1919del |