Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.134148767C>T , CM000673.2:g.134148767C>T | GRCh38 |
| NC_000011.9:g.134018662C>T , CM000673.1:g.134018662C>T | GRCh37 |
| NC_000011.8:g.133523872C>T | NCBI36 |
| NG_028348.1:g.84843C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299106.9:c.846C>T MANE Select | ENSP00000299106.4:p.Tyr282= | |
| ENST00000299106.8:c.846C>T | ENSP00000299106.4:p.Tyr282= | |
| ENST00000441717.3:c.693C>T | ENSP00000395742.3:p.Tyr231= | |
| ENST00000533711.1:n.883C>T | ||
| NM_001205329.1:c.693C>T | NP_001192258.1:p.Tyr231= | |
| NM_032801.4:c.846C>T | NP_116190.3:p.Tyr282= | |
| NM_032801.5:c.846C>T MANE Select | NP_116190.3:p.Tyr282= | |
| NM_001205329.2:c.693C>T | NP_001192258.1:p.Tyr231= |