HGVS | Genome Assembly |
---|---|
NC_000002.12:g.88859766T>A , CM000664.2:g.88859766T>A | GRCh38 |
NC_000002.11:g.89159278T>A , CM000664.1:g.89159278T>A | GRCh37 |
NC_000002.10:g.88940393T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377423.6:c.389-2083A>T (IGKV1-12) | ENSP00000480537.2:n.389-2083A>T | |
ENST00000430694.5:c.37+1120A>T (IGKC) | ENSP00000481923.2:n.37+1120A>T | |
ENST00000610638.3:c.397+1759A>T (IGKC) | ENSP00000484499.3:n.397+1759A>T | |
ENST00000634828.1:c.382+1759A>T (IGKV1-8) | ENSP00000489500.1:n.382+1759A>T |