HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43886879_43886880del , CM000664.2:g.43886879_43886880del | GRCh38 |
NC_000002.11:g.44114018_44114019del , CM000664.1:g.44114018_44114019del | GRCh37 |
NC_000002.10:g.43967522_43967523del | NCBI36 |
NG_008247.1:g.114129_114130del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2675_2676del | ||
ENST00000684454.1:n.9772_9773del | ||
ENST00000260665.12:c.*1723_*1724del MANE Select | ENSP00000260665.7:n.*1723_*1724del | |
ENST00000260665.11:c.*1723_*1724del | ENSP00000260665.7:n.*1723_*1724del | |
NM_133259.3:c.*1723_*1724del | NP_573566.2:n.*1723_*1724del | |
XR_002958896.1:n.6090_6091del | ||
NM_133259.4:c.*1723_*1724del MANE Select | NP_573566.2:n.*1723_*1724del |