Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20242470G= , CM000684.2:g.20242470G= | GRCh38 |
| NC_000022.10:g.20229993G= , CM000684.1:g.20229993G= | GRCh37 |
| NC_000022.9:g.18609993G= | NCBI36 |
| NG_012176.1:g.30824C= | |
| NG_012176.2:g.30824C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000043402.8:c.663C= MANE Select | ENSP00000043402.7:p.Ala221= | |
| ENST00000043402.7:c.663C= | ENSP00000043402.7:p.Ala221= | |
| ENST00000416372.5:c.722C= | ||
| ENST00000425986.1:c.920C= | ||
| NM_023004.5:c.663C= | NP_075380.1:p.Ala221= | |
| NM_023004.6:c.663C= MANE Select | NP_075380.1:p.Ala221= |