Canonical Allele Identifier:
CA1482797938
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542866A= , CM000666.2:g.105542866A= | GRCh38 |
| NC_000004.11:g.106464023A= , CM000666.1:g.106464023A= | GRCh37 |
| NC_000004.10:g.106683472A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.296-157T= | ||
| XR_939039.1:n.456-157T= | ||
| XR_939040.1:n.296-1390T= | ||
| XR_001741410.1:n.311-157T= | ||
| XR_001741411.1:n.787-157T= | ||
| XR_001741412.1:n.311-157T= | ||
| XR_001741413.1:n.311-157T= | ||
| XR_001741414.1:n.311-157T= | ||
| XR_939038.2:n.311-157T= | ||
| XR_939040.2:n.311-1390T= |