Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10412876A= , CM000682.2:g.10412876A= | GRCh38 |
| NC_000020.10:g.10393524A= , CM000682.1:g.10393524A= | GRCh37 |
| NC_000020.9:g.10341524A= | NCBI36 |
| NG_009109.1:g.26343T= | |
| NG_009109.2:g.26343T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651692.1:c.639T= | ENSP00000498849.1:p.Thr213= | |
| ENST00000652676.1:n.459-176T= | ||
| ENST00000347364.7:c.639T= MANE Select | ENSP00000246062.4:p.Thr213= | |
| ENST00000399054.6:c.639T= | ENSP00000382008.2:p.Thr213= | |
| NM_018848.3:c.639T= | NP_061336.1:p.Thr213= | |
| NM_170784.2:c.639T= | NP_740754.1:p.Thr213= | |
| NR_072977.1:n.364-4073T= | ||
| NR_072977.2:n.347-4073T= | ||
| NM_170784.3:c.639T= MANE Select | NP_740754.1:p.Thr213= |