HGVS | Genome Assembly |
---|---|
NC_000002.12:g.88859362A>G , CM000664.2:g.88859362A>G | GRCh38 |
NC_000002.11:g.89158875A>G , CM000664.1:g.89158875A>G | GRCh37 |
NC_000002.10:g.88939990A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377423.6:c.389-1679T>C (IGKV1-12) | ENSP00000480537.2:n.389-1679T>C | |
ENST00000430694.5:c.37+1524T>C (IGKC) | ENSP00000481923.2:n.37+1524T>C | |
ENST00000610638.3:c.398-1679T>C (IGKC) | ENSP00000484499.3:n.398-1679T>C | |
ENST00000634828.1:c.383-1679T>C (IGKV1-8) | ENSP00000489500.1:n.383-1679T>C |