Linked Data
dbSNP Id:
rs556771940
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88859655C>G , CM000664.2:g.88859655C>G | GRCh38 |
| NC_000002.11:g.89159167C>G , CM000664.1:g.89159167C>G | GRCh37 |
| NC_000002.10:g.88940282C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377423.6:c.389-1972G>C (IGKV1-12) | ENSP00000480537.2:n.389-1972G>C | |
| ENST00000430694.5:c.37+1231G>C (IGKC) | ENSP00000481923.2:n.37+1231G>C | |
| ENST00000610638.3:c.397+1870G>C (IGKC) | ENSP00000484499.3:n.397+1870G>C | |
| ENST00000634828.1:c.382+1870G>C (IGKV1-8) | ENSP00000489500.1:n.382+1870G>C |