Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30207451A= , CM000679.2:g.30207451A= | GRCh38 |
| NC_000017.10:g.28534469A= , CM000679.1:g.28534469A= | GRCh37 |
| NC_000017.9:g.25558595A= | NCBI36 |
| NG_011747.2:g.33486T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001045.6:c.1650+281T= MANE Select | NP_001036.1:n.1650+281T= |
| ENST00000650711.1:c.1650+281T= MANE Select | ENSP00000498537.1:n.1650+281T= |
| NM_001045.5:c.1650+281T= | NP_001036.1:n.1650+281T= |
| ENST00000261707.7:c.1650+281T= | ENSP00000261707.3:n.1650+281T= |
| ENST00000394821.2:c.1650+281T= | ENSP00000378298.2:n.1650+281T= |
| ENST00000401766.6:c.1650+281T= | ENSP00000385822.2:n.1650+281T= |
| ENST00000579221.5:c.291+281T= |