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