Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586568A>G , CM000679.2:g.41586568A>G | GRCh38 |
| NC_000017.10:g.39742820A>G , CM000679.1:g.39742820A>G | GRCh37 |
| NC_000017.9:g.36996346A>G | NCBI36 |
| NG_008624.1:g.5328T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.267T>C MANE Select | ENSP00000167586.6:p.Gly89= | |
| ENST00000167586.6:c.267T>C | ENSP00000167586.6:p.Gly89= | |
| NM_000526.4:c.267T>C | NP_000517.2:p.Gly89= | |
| NM_000526.5:c.267T>C MANE Select | NP_000517.3:p.Gly89= |