Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116822655T= , CM000673.2:g.116822655T= | GRCh38 |
| NC_000011.9:g.116693371T= , CM000673.1:g.116693371T= | GRCh37 |
| NC_000011.8:g.116198581T= | NCBI36 |
| NG_012044.1:g.5641A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357780.5:c.176+4A= MANE Select | ENSP00000350425.3:n.176+4A= | |
| ENST00000357780.4:c.176+4A= | ENSP00000350425.3:n.176+4A= | |
| NM_000482.3:c.176+4A= | NP_000473.2:n.176+4A= | |
| NM_000482.4:c.176+4A= MANE Select | NP_000473.2:n.176+4A= |