Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862867T= , CM000666.2:g.4862867T= | GRCh38 |
| NC_000004.11:g.4864594T= , CM000666.1:g.4864594T= | GRCh37 |
| NC_000004.10:g.4915495T= | NCBI36 |
| NG_008121.1:g.8203T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.636T= MANE Select | ENSP00000372170.4:p.Thr212= | |
| ENST00000382723.4:c.636T= | ENSP00000372170.4:p.Thr212= | |
| ENST00000468421.1:n.348T= | ||
| NM_002448.3:c.636T= MANE Select | NP_002439.2:p.Thr212= |