Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031389T= , CM000667.2:g.135031389T= | GRCh38 |
| NC_000005.9:g.134367079T= , CM000667.1:g.134367079T= | GRCh37 |
| NC_000005.8:g.134394978T= | NCBI36 |
| NG_012114.1:g.7886A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.289A= MANE Select | ENSP00000265340.6:p.Thr97= | |
| ENST00000265340.11:c.289A= | ENSP00000265340.6:p.Thr97= | |
| ENST00000502676.1:c.289A= | ENSP00000423624.1:p.Thr97= | |
| ENST00000503586.1:c.411A= | ||
| ENST00000504936.1:n.622A= | ||
| ENST00000506438.5:c.289A= | ENSP00000427542.1:p.Thr97= | |
| ENST00000507253.5:c.289A= | ENSP00000422908.1:p.Thr97= | |
| NM_002653.4:c.289A= | NP_002644.4:p.Thr97= | |
| NM_002653.5:c.289A= MANE Select | NP_002644.4:p.Thr97= |