Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8076653T= , CM000679.2:g.8076653T= | GRCh38 |
| NC_000017.10:g.7979971T= , CM000679.1:g.7979971T= | GRCh37 |
| NC_000017.9:g.7920696T= | NCBI36 |
| NG_007099.1:g.16051A= | |
| NG_007099.2:g.16064A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1362+4A= MANE Select | ENSP00000497784.1:n.1362+4A= | |
| ENST00000649809.1:c.426+4A= | ENSP00000496845.1:n.426+4A= | |
| ENST00000319144.4:c.1362+4A= | ENSP00000315167.4:n.1362+4A= | |
| ENST00000577351.5:n.309+4A= | ||
| ENST00000583276.5:n.746+4A= | ||
| ENST00000584116.1:n.618+4A= | ||
| NM_001139.2:c.1362+4A= | NP_001130.1:n.1362+4A= | |
| NM_001139.3:c.1362+4A= MANE Select | NP_001130.1:n.1362+4A= |