Canonical Allele Identifier:
CA1482797490
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542504T= , CM000666.2:g.105542504T= | GRCh38 |
| NC_000004.11:g.106463661T= , CM000666.1:g.106463661T= | GRCh37 |
| NC_000004.10:g.106683110T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.501A= | ||
| XR_939039.1:n.661A= | ||
| XR_939040.1:n.296-1028A= | ||
| XR_001741410.1:n.516A= | ||
| XR_001741411.1:n.992A= | ||
| XR_001741412.1:n.449+67A= | ||
| XR_001741413.1:n.516A= | ||
| XR_001741414.1:n.449+67A= | ||
| XR_939038.2:n.516A= | ||
| XR_939040.2:n.311-1028A= |