Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818822A= , CM000671.2:g.129818822A= | GRCh38 |
| NC_000009.11:g.132581101A= , CM000671.1:g.132581101A= | GRCh37 |
| NC_000009.10:g.131620922A= | NCBI36 |
| NG_008049.1:g.10341T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.543T= MANE Select | ENSP00000345719.4:p.Asp181= | |
| ENST00000651202.1:c.639T= | ENSP00000498222.1:p.Asp213= | |
| ENST00000351698.4:c.543T= | ENSP00000345719.4:p.Asp181= | |
| ENST00000473604.2:n.653T= | ||
| NM_000113.2:c.543T= | NP_000104.1:p.Asp181= | |
| XR_929731.1:n.703T= | ||
| XR_929731.3:n.571T= | ||
| NM_000113.3:c.543T= MANE Select | NP_000104.1:p.Asp181= |