Canonical Allele Identifier:
CA2566578985
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283691C>A , CM000669.2:g.24283691C>A | GRCh38 |
| NC_000007.13:g.24323310C>A , CM000669.1:g.24323310C>A | GRCh37 |
| NC_000007.12:g.24289835C>A | NCBI36 |
| NG_016148.1:g.4504C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_017012910.1:c.42-27992G>T | XP_016868399.1:n.42-27992G>T | |
| XM_017012911.1:c.42-27992G>T | XP_016868400.1:n.42-27992G>T | |
| XR_001745121.1:n.473+35666G>T | ||
| XR_001745122.1:n.345-86662G>T | ||
| XR_001745123.1:n.473+35666G>T | ||
| XR_001745124.1:n.473+35666G>T | ||
| XR_001745125.1:n.473+35666G>T | ||
| XR_001745126.1:n.473+35666G>T | ||
| XR_001745127.1:n.345-27992G>T | ||
| XR_001745129.1:n.473+35666G>T | ||
| XR_001745130.1:n.473+35666G>T | ||
| XR_001745131.1:n.473+35666G>T | ||
| XR_001745132.1:n.473+35666G>T |