Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36663064G>A , CM000676.2:g.36663064G>A | GRCh38 |
| NC_000014.8:g.37132269G>A , CM000676.1:g.37132269G>A | GRCh37 |
| NC_000014.7:g.36202020G>A | NCBI36 |
| NG_013357.1:g.10497G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361487.7:c.172G>A MANE Select | ENSP00000355245.6:p.Ala58Thr | |
| ENST00000555639.2:c.172G>A | ENSP00000501203.1:p.Ala58Thr | |
| ENST00000361487.6:c.172G>A | ENSP00000355245.6:p.Ala58Thr | |
| ENST00000402703.6:c.172G>A | ENSP00000384817.2:p.Ala58Thr | |
| ENST00000554201.1:c.-390G>A | ENSP00000450434.1:n.-390G>A | |
| ENST00000555639.1:n.474G>A | ||
| NM_006194.3:c.172G>A | NP_006185.1:p.Ala58Thr | |
| NM_001372076.1:c.172G>A MANE Select | NP_001359005.1:p.Ala58Thr | |
| NM_006194.4:c.172G>A | NP_006185.1:p.Ala58Thr |