Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22721145T= , CM000669.2:g.22721145T= | GRCh38 |
| NC_000007.13:g.22760764T= , CM000669.1:g.22760764T= | GRCh37 |
| NC_000007.12:g.22727289T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+6423A= |