Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868280C>T , CM000663.2:g.23868280C>T | GRCh38 |
| NC_000001.10:g.24194770C>T , CM000663.1:g.24194770C>T | GRCh37 |
| NC_000001.9:g.24067357C>T | NCBI36 |
| NG_013346.1:g.5090G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000147.5:c.7G>A MANE Select | NP_000138.2:p.Ala3Thr |
| ENST00000374479.4:c.7G>A MANE Select | ENSP00000363603.3:p.Ala3Thr |
| NM_000147.4:c.7G>A | NP_000138.2:p.Ala3Thr |
| NR_174379.1:n.11G>A | |
| NR_174380.1:n.11G>A | |
| NR_174381.1:n.11G>A | |
| NR_174382.1:n.11G>A | |
| ENST00000374479.3:c.7G>A | ENSP00000363603.3:p.Ala3Thr |
| XM_005245821.1:c.-543G>A | XP_005245878.1:n.-543G>A |
| XM_005245821.3:c.-543G>A | XP_005245878.1:n.-543G>A |