Linked Data
dbSNP Id:
rs1696250100
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233250213T>C , CM000664.2:g.233250213T>C | GRCh38 |
| NC_000002.11:g.234158859T>C , CM000664.1:g.234158859T>C | GRCh37 |
| NC_000002.10:g.233823598T>C | NCBI36 |
| NG_023038.1:g.3643T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000431917.5:c.-137-5889T>C | ENSP00000397512.1:n.-137-5889T>C |