Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.73196460T= , CM000679.2:g.73196460T= | GRCh38 |
| NC_000017.10:g.71192599T= , CM000679.1:g.71192599T= | GRCh37 |
| NC_000017.9:g.68704194T= | NCBI36 |
| NG_008971.1:g.8427T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299886.9:c.316-47T= MANE Select | ENSP00000299886.4:n.316-47T= | |
| ENST00000299886.8:c.316-47T= | ENSP00000299886.4:n.316-47T= | |
| ENST00000438720.7:c.314-47T= | ||
| ENST00000582587.2:c.293-27T= | ||
| ENST00000618996.4:c.316-47T= | ENSP00000479450.1:n.316-47T= | |
| NM_018714.2:c.316-47T= | NP_061184.1:n.316-47T= | |
| NM_018714.3:c.316-47T= MANE Select | NP_061184.1:n.316-47T= |