Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10645009T= , CM000682.2:g.10645009T= | GRCh38 |
| NC_000020.10:g.10625657T= , CM000682.1:g.10625657T= | GRCh37 |
| NC_000020.9:g.10573657T= | NCBI36 |
| NG_007496.1:g.34038A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2228-30A= MANE Select | ENSP00000254958.4:n.2228-30A= | |
| ENST00000617965.2:n.2817-30A= | ||
| ENST00000254958.9:c.2228-30A= | ENSP00000254958.4:n.2228-30A= | |
| ENST00000423891.6:n.2094-30A= | ||
| ENST00000488480.2:n.625-30A= | ||
| NM_000214.2:c.2228-30A= | NP_000205.1:n.2228-30A= | |
| NM_000214.3:c.2228-30A= MANE Select | NP_000205.1:n.2228-30A= |