Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.77462742G= , CM000668.2:g.77462742G= | GRCh38 |
| NC_000006.11:g.78172459G= , CM000668.1:g.78172459G= | GRCh37 |
| NC_000006.10:g.78229178G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000863.3:c.662C= MANE Select | NP_000854.1:p.Thr221= |
| ENST00000369947.5:c.662C= MANE Select | ENSP00000358963.3:p.Thr221= |
| NM_000863.1:c.662C= | NP_000854.1:p.Thr221= |
| NM_000863.2:c.662C= | NP_000854.1:p.Thr221= |
| ENST00000369947.3:c.662C= | ENSP00000358963.2:p.Thr221= |
| XR_942706.1:n.545-11784G= | |
| XR_942707.1:n.545-11784G= | |
| XR_942708.1:n.545-11784G= | |
| XR_942708.2:n.545-11784G= | |
| XR_942709.1:n.545-11784G= |