Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99149921C>A , CM000666.2:g.99149921C>A | GRCh38 |
| NC_000004.11:g.100071078C>A , CM000666.1:g.100071078C>A | GRCh37 |
| NC_000004.10:g.100290101C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504581.1:n.170-7141G>T | ||
| NR_037884.1:n.680-4624C>A |