HGVS | Genome Assembly |
---|---|
NC_000002.12:g.88859657_88859660del , CM000664.2:g.88859657_88859660del | GRCh38 |
NC_000002.11:g.89159169_89159172del , CM000664.1:g.89159169_89159172del | GRCh37 |
NC_000002.10:g.88940284_88940287del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377423.6:c.389-1977_389-1974del (IGKV1-12) | ENSP00000480537.2:n.389-1977_389-1974del | |
ENST00000430694.5:c.37+1226_37+1229del (IGKC) | ENSP00000481923.2:n.37+1226_37+1229del | |
ENST00000610638.3:c.397+1865_397+1868del (IGKC) | ENSP00000484499.3:n.397+1865_397+1868del | |
ENST00000634828.1:c.382+1865_382+1868del (IGKV1-8) | ENSP00000489500.1:n.382+1865_382+1868del |