Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94001012T>A , CM000663.2:g.94001012T>A | GRCh38 |
| NC_000001.10:g.94466568T>A , CM000663.1:g.94466568T>A | GRCh37 |
| NC_000001.9:g.94239156T>A | NCBI36 |
| NG_009073.1:g.125138A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6376A>T MANE Select | ENSP00000359245.3:p.Thr2126Ser | |
| ENST00000370225.3:c.6376A>T | ENSP00000359245.3:p.Thr2126Ser | |
| ENST00000536513.5:c.2752A>T | ENSP00000439707.2:p.Thr918Ser | |
| NM_000350.2:c.6376A>T | NP_000341.2:p.Thr2126Ser | |
| NM_000350.3:c.6376A>T MANE Select | NP_000341.2:p.Thr2126Ser |