Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21307838T>G , CM000676.2:g.21307838T>G | GRCh38 |
| NC_000014.8:g.21775997T>G , CM000676.1:g.21775997T>G | GRCh37 |
| NC_000014.7:g.20845837T>G | NCBI36 |
| NG_008933.1:g.24862T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020366.4:c.906+2T>G MANE Select | NP_065099.3:n.906+2T>G |
| ENST00000400017.7:c.906+2T>G MANE Select | ENSP00000382895.2:n.906+2T>G |
| NM_020366.3:c.906+2T>G | NP_065099.3:n.906+2T>G |
| ENST00000400017.6:c.906+2T>G | ENSP00000382895.2:n.906+2T>G |
| ENST00000556336.5:c.825+2T>G | ENSP00000450445.1:n.825+2T>G |
| ENST00000557771.5:c.825+2T>G | ENSP00000451219.1:n.825+2T>G |
| XM_011536983.1:c.873+2T>G | XP_011535285.1:n.873+2T>G |