Linked Data
dbSNP Id:
rs974895308
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216998764T>C , CM000664.2:g.216998764T>C | GRCh38 |
| NC_000002.11:g.217863487T>C , CM000664.1:g.217863487T>C | GRCh37 |
| NC_000002.10:g.217571732T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923881.1:n.299+4746T>C | ||
| XR_923883.1:n.294+4746T>C | ||
| XR_923885.1:n.862+4746T>C | ||
| XR_923886.1:n.300-2283T>C | ||
| XR_923887.1:n.299+4746T>C | ||
| XR_001739169.1:n.11844+4746T>C | ||
| XR_001739170.2:n.8480+4746T>C | ||
| XR_001739171.2:n.8347+4746T>C |