Canonical Allele Identifier:
CA1932888191
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102902701T= , CM000672.2:g.102902701T= | GRCh38 |
| NC_000010.10:g.104662458T= , CM000672.1:g.104662458T= | GRCh37 |
| NC_000010.9:g.104652448T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017017027.1:c.447-2191A= | XP_016872516.1:n.447-2191A= | |
| XR_001747577.1:n.169-2191A= | ||
| XR_001747578.1:n.345-2191A= | ||
| NR_160733.1:n.169-2191A= |