Canonical Allele Identifier:
CA2549612966
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30201830T>G , CM000672.2:g.30201830T>G | GRCh38 |
| NC_000010.10:g.30490759T>G , CM000672.1:g.30490759T>G | GRCh37 |
| NC_000010.9:g.30530765T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_930791.1:n.1193-1657T>G | ||
| XR_930791.2:n.1449-1657T>G |