Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10413346T= , CM000682.2:g.10413346T= | GRCh38 |
| NC_000020.10:g.10393994T= , CM000682.1:g.10393994T= | GRCh37 |
| NC_000020.9:g.10341994T= | NCBI36 |
| NG_009109.1:g.25873A= | |
| NG_009109.2:g.25873A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_170784.3:c.169A= MANE Select | NP_740754.1:p.Thr57= |
| ENST00000347364.7:c.169A= MANE Select | ENSP00000246062.4:p.Thr57= |
| NM_018848.3:c.169A= | NP_061336.1:p.Thr57= |
| NM_170784.2:c.169A= | NP_740754.1:p.Thr57= |
| NR_072977.1:n.364-4543A= | |
| NR_072977.2:n.347-4543A= | |
| ENST00000399054.6:c.169A= | ENSP00000382008.2:p.Thr57= |
| ENST00000651692.1:c.169A= | ENSP00000498849.1:p.Thr57= |
| ENST00000652676.1:n.458+450A= |