Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116822748C= , CM000673.2:g.116822748C= | GRCh38 |
| NC_000011.9:g.116693464C= , CM000673.1:g.116693464C= | GRCh37 |
| NC_000011.8:g.116198674C= | NCBI36 |
| NG_012044.1:g.5548G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000482.4:c.87G= MANE Select | NP_000473.2:p.Thr29= |
| ENST00000357780.5:c.87G= MANE Select | ENSP00000350425.3:p.Thr29= |
| NM_000482.3:c.87G= | NP_000473.2:p.Thr29= |
| ENST00000357780.4:c.87G= | ENSP00000350425.3:p.Thr29= |