Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24795012C>T , CM000666.2:g.24795012C>T | GRCh38 |
| NC_000004.11:g.24796634C>T , CM000666.1:g.24796634C>T | GRCh37 |
| NC_000004.10:g.24405732C>T | NCBI36 |
| NG_012213.1:g.4550C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-16-4494C>T | ENSP00000472134.1:n.-16-4494C>T |