HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43886942_43886943insTT , CM000664.2:g.43886942_43886943insTT | GRCh38 |
NC_000002.11:g.44114081_44114082insTT , CM000664.1:g.44114081_44114082insTT | GRCh37 |
NC_000002.10:g.43967585_43967586insTT | NCBI36 |
NG_008247.1:g.114063_114064insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2609_2610insAA | ||
ENST00000684454.1:n.9706_9707insAA | ||
ENST00000260665.12:c.*1657_*1658insAA MANE Select | ENSP00000260665.7:n.*1657_*1658insAA | |
ENST00000260665.11:c.*1657_*1658insAA | ENSP00000260665.7:n.*1657_*1658insAA | |
NM_133259.3:c.*1657_*1658insAA | NP_573566.2:n.*1657_*1658insAA | |
XR_002958896.1:n.6024_6025insAA | ||
NM_133259.4:c.*1657_*1658insAA MANE Select | NP_573566.2:n.*1657_*1658insAA |