Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8076470T>A , CM000679.2:g.8076470T>A | GRCh38 |
| NC_000017.10:g.7979788T>A , CM000679.1:g.7979788T>A | GRCh37 |
| NC_000017.9:g.7920513T>A | NCBI36 |
| NG_007099.1:g.16234A>T | |
| NG_007099.2:g.16247A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1363-126A>T MANE Select | ENSP00000497784.1:n.1363-126A>T | |
| ENST00000649809.1:c.427-126A>T | ENSP00000496845.1:n.427-126A>T | |
| ENST00000319144.4:c.1363-126A>T | ENSP00000315167.4:n.1363-126A>T | |
| ENST00000577351.5:n.310-126A>T | ||
| ENST00000583276.5:n.747-126A>T | ||
| ENST00000584116.1:n.619-126A>T | ||
| NM_001139.2:c.1363-126A>T | NP_001130.1:n.1363-126A>T | |
| NM_001139.3:c.1363-126A>T MANE Select | NP_001130.1:n.1363-126A>T |