Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10672772T>C , CM000682.2:g.10672772T>C | GRCh38 |
| NC_000020.10:g.10653420T>C , CM000682.1:g.10653420T>C | GRCh37 |
| NC_000020.9:g.10601420T>C | NCBI36 |
| NG_007496.1:g.6275A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.316A>G MANE Select | NP_000205.1:p.Thr106Ala |
| ENST00000254958.10:c.316A>G MANE Select | ENSP00000254958.4:p.Thr106Ala |
| NM_000214.2:c.316A>G | NP_000205.1:p.Thr106Ala |
| ENST00000254958.9:c.316A>G | ENSP00000254958.4:p.Thr106Ala |