Canonical Allele Identifier:
CA2580594248
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283791T>G , CM000669.2:g.24283791T>G | GRCh38 |
| NC_000007.13:g.24323410T>G , CM000669.1:g.24323410T>G | GRCh37 |
| NC_000007.12:g.24289935T>G | NCBI36 |
| NG_016148.1:g.4604T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017012910.1:c.42-28092A>C | XP_016868399.1:n.42-28092A>C | |
| XM_017012911.1:c.42-28092A>C | XP_016868400.1:n.42-28092A>C | |
| XR_001745121.1:n.473+35566A>C | ||
| XR_001745122.1:n.345-86762A>C | ||
| XR_001745123.1:n.473+35566A>C | ||
| XR_001745124.1:n.473+35566A>C | ||
| XR_001745125.1:n.473+35566A>C | ||
| XR_001745126.1:n.473+35566A>C | ||
| XR_001745127.1:n.345-28092A>C | ||
| XR_001745129.1:n.473+35566A>C | ||
| XR_001745130.1:n.473+35566A>C | ||
| XR_001745131.1:n.473+35566A>C | ||
| XR_001745132.1:n.473+35566A>C |