HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43886918_43886919insT , CM000664.2:g.43886918_43886919insT | GRCh38 |
NC_000002.11:g.44114057_44114058insT , CM000664.1:g.44114057_44114058insT | GRCh37 |
NC_000002.10:g.43967561_43967562insT | NCBI36 |
NG_008247.1:g.114087_114088insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2633_2634insA | ||
ENST00000684454.1:n.9730_9731insA | ||
ENST00000260665.12:c.*1681_*1682insA MANE Select | ENSP00000260665.7:n.*1681_*1682insA | |
ENST00000260665.11:c.*1681_*1682insA | ENSP00000260665.7:n.*1681_*1682insA | |
NM_133259.3:c.*1681_*1682insA | NP_573566.2:n.*1681_*1682insA | |
XR_002958896.1:n.6048_6049insA | ||
NM_133259.4:c.*1681_*1682insA MANE Select | NP_573566.2:n.*1681_*1682insA |