Linked Data
dbSNP Id:
rs1940385618
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.40197332A>G , CM000674.2:g.40197332A>G | GRCh38 |
| NC_000012.11:g.40591134A>G , CM000674.1:g.40591134A>G | GRCh37 |
| NC_000012.10:g.38877401A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000416796.5:c.-63+559A>G | ENSP00000398726.1:n.-63+559A>G |