Linked Data
dbSNP Id:
rs1696253616
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233250280A>C , CM000664.2:g.233250280A>C | GRCh38 |
| NC_000002.11:g.234158926A>C , CM000664.1:g.234158926A>C | GRCh37 |
| NC_000002.10:g.233823665A>C | NCBI36 |
| NG_023038.1:g.3710A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431917.5:c.-137-5822A>C | ENSP00000397512.1:n.-137-5822A>C |