Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216148178A= , CM000664.2:g.216148178A= | GRCh38 |
| NC_000002.11:g.217012901A= , CM000664.1:g.217012901A= | GRCh37 |
| NC_000002.10:g.216721146A= | NCBI36 |
| NG_029780.1:g.43882A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392132.7:c.1572A= MANE Select | ENSP00000375977.2:p.Thr524= | |
| ENST00000392132.6:c.1572A= | ENSP00000375977.2:p.Thr524= | |
| ENST00000392133.7:c.1572A= | ENSP00000375978.3:p.Thr524= | |
| ENST00000460284.5:n.2114A= | ||
| NM_021141.3:c.1572A= | NP_066964.1:p.Thr524= | |
| NM_021141.4:c.1572A= MANE Select | NP_066964.1:p.Thr524= |