Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013332G= , CM000685.2:g.25013332G= | GRCh38 |
| NC_000023.10:g.25031449G= , CM000685.1:g.25031449G= | GRCh37 |
| NC_000023.9:g.24941370G= | NCBI36 |
| NG_008281.1:g.7617C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379044.5:c.663C= MANE Select | ENSP00000368332.4:p.Thr221= | |
| ENST00000379044.4:c.663C= | ENSP00000368332.4:p.Thr221= | |
| NM_139058.2:c.663C= | NP_620689.1:p.Thr221= | |
| NM_139058.3:c.663C= MANE Select | NP_620689.1:p.Thr221= |