Canonical Allele Identifier:
CA1674885731
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812479T= , CM000668.2:g.155812479T= | GRCh38 |
| NC_000006.11:g.156133613T= , CM000668.1:g.156133613T= | GRCh37 |
| NC_000006.10:g.156175305T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19060T= | ||
| XR_943146.1:n.645-440A= | ||
| XR_001744423.1:n.699-440A= | ||
| XR_001744424.1:n.79+19060T= |