Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99149740T= , CM000666.2:g.99149740T= | GRCh38 |
| NC_000004.11:g.100070897T= , CM000666.1:g.100070897T= | GRCh37 |
| NC_000004.10:g.100289920T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504581.1:n.170-6960A= | ||
| NR_037884.1:n.680-4805T= |