Linked Data
dbSNP Id:
rs1763680986
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31008775T>C , CM000668.2:g.31008775T>C | GRCh38 |
| NC_000006.11:g.30976552T>C , CM000668.1:g.30976552T>C | GRCh37 |
| NC_000006.10:g.31084531T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001198815.1:c.-37-1895T>C | NP_001185744.1:n.-37-1895T>C | |
| NM_001318484.1:c.8-1930T>C | NP_001305413.1:n.8-1930T>C |