Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35797486T>G , CM000668.2:g.35797486T>G | GRCh38 |
| NC_000006.11:g.35765263T>G , CM000668.1:g.35765263T>G | GRCh37 |
| NC_000006.10:g.35873241T>G | NCBI36 |
| NG_012184.3:g.5281T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651132.1:c.-255+27T>G | ENSP00000498322.1:n.-255+27T>G | |
| XM_011514403.1:c.-135+27T>G | XP_011512705.1:n.-135+27T>G |