Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658464A= , CM000682.2:g.10658464A= | GRCh38 |
| NC_000020.10:g.10639112A= , CM000682.1:g.10639112A= | GRCh37 |
| NC_000020.9:g.10587112A= | NCBI36 |
| NG_007496.1:g.20583T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.694+4T= MANE Select | ENSP00000254958.4:n.694+4T= | |
| ENST00000254958.9:c.694+4T= | ENSP00000254958.4:n.694+4T= | |
| ENST00000423891.6:n.560+4T= | ||
| NM_000214.2:c.694+4T= | NP_000205.1:n.694+4T= | |
| NM_000214.3:c.694+4T= MANE Select | NP_000205.1:n.694+4T= |