Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232543052G>A , CM000664.2:g.232543052G>A | GRCh38 |
| NC_000002.11:g.233407762G>A , CM000664.1:g.233407762G>A | GRCh37 |
| NC_000002.10:g.233116006G>A | NCBI36 |
| NG_012954.1:g.8326G>A | |
| NG_012954.2:g.8361G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651502.1:c.775G>A MANE Select | ENSP00000498757.1:p.Ala259Thr | |
| ENST00000389492.3:c.619G>A | ENSP00000374143.3:p.Ala207Thr | |
| ENST00000389494.7:c.775G>A | ENSP00000374145.3:p.Ala259Thr | |
| NM_005199.4:c.775G>A | NP_005190.4:p.Ala259Thr | |
| NM_005199.5:c.775G>A MANE Select | NP_005190.4:p.Ala259Thr |