Canonical Allele Identifier:
CA1694873537
Gene:
Linked Data
dbSNP Id:
rs1787248101
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283915A>G , CM000669.2:g.24283915A>G | GRCh38 |
| NC_000007.13:g.24323534A>G , CM000669.1:g.24323534A>G | GRCh37 |
| NC_000007.12:g.24290059A>G | NCBI36 |
| NG_016148.1:g.4728A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017012910.1:c.42-28216T>C | XP_016868399.1:n.42-28216T>C | |
| XM_017012911.1:c.42-28216T>C | XP_016868400.1:n.42-28216T>C | |
| XR_001745121.1:n.473+35442T>C | ||
| XR_001745122.1:n.345-86886T>C | ||
| XR_001745123.1:n.473+35442T>C | ||
| XR_001745124.1:n.473+35442T>C | ||
| XR_001745125.1:n.473+35442T>C | ||
| XR_001745126.1:n.473+35442T>C | ||
| XR_001745127.1:n.345-28216T>C | ||
| XR_001745129.1:n.473+35442T>C | ||
| XR_001745130.1:n.473+35442T>C | ||
| XR_001745131.1:n.473+35442T>C | ||
| XR_001745132.1:n.473+35442T>C |