Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233235T= , CM000667.2:g.55233235T= | GRCh38 |
| NC_000005.9:g.54529063T= , CM000667.1:g.54529063T= | GRCh37 |
| NC_000005.8:g.54564820T= | NCBI36 |
| NG_034201.1:g.5483A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.289A= MANE Select | ENSP00000282572.4:p.Thr97= | |
| ENST00000282572.4:c.289A= | ENSP00000282572.4:p.Thr97= | |
| ENST00000501463.2:c.289A= | ENSP00000422485.1:p.Thr97= | |
| NM_021147.4:c.289A= | NP_066970.3:p.Thr97= | |
| NR_125346.1:n.483A= | ||
| NR_125347.1:n.483A= | ||
| NM_021147.5:c.289A= MANE Select | NP_066970.3:p.Thr97= | |
| NR_125346.2:n.374A= | ||
| NR_125347.2:n.374A= |