Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177080G>A , CM000678.2:g.177080G>A | GRCh38 |
| NC_000016.9:g.227079G>A , CM000678.1:g.227079G>A | GRCh37 |
| NC_000016.8:g.167079G>A | NCBI36 |
| NG_000006.1:g.37943G>A | |
| NG_059186.1:g.5430G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320868.9:c.247G>A MANE Select | ENSP00000322421.5:p.Ala83Thr | |
| ENST00000397797.1:c.151G>A | ENSP00000380899.1:p.Ala51Thr | |
| ENST00000472694.1:n.383G>A | ||
| ENST00000487791.1:n.216G>A | ||
| NM_000558.4:c.247G>A | NP_000549.1:p.Ala83Thr | |
| NM_000558.5:c.247G>A MANE Select | NP_000549.1:p.Ala83Thr |