Canonical Allele Identifier:
CA1674885899
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812659T= , CM000668.2:g.155812659T= | GRCh38 |
| NC_000006.11:g.156133793T= , CM000668.1:g.156133793T= | GRCh37 |
| NC_000006.10:g.156175485T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_943142.1:n.79+19240T= | ||
| XR_943146.1:n.645-620A= | ||
| XR_001744423.1:n.699-620A= | ||
| XR_001744424.1:n.79+19240T= |