Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615609T>C , CM000668.2:g.151615609T>C | GRCh38 |
| NC_000006.11:g.151936744T>C , CM000668.1:g.151936744T>C | GRCh37 |
| NC_000006.10:g.151978437T>C | NCBI36 |
| NG_021198.1:g.126570T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1877T>C MANE Select | ENSP00000239374.6:p.Ile626Thr | |
| ENST00000239374.7:c.1877T>C | ENSP00000239374.6:p.Ile626Thr | |
| NM_025059.3:c.1877T>C | NP_079335.2:p.Ile626Thr | |
| XM_011536147.1:c.1895T>C | XP_011534449.1:p.Ile632Thr | |
| XM_011536148.1:c.1694T>C | XP_011534450.1:p.Ile565Thr | |
| XM_011536147.2:c.1895T>C | XP_011534449.1:p.Ile632Thr | |
| XM_011536148.2:c.1694T>C | XP_011534450.1:p.Ile565Thr | |
| XR_001743865.1:n.129+1112A>G | ||
| NM_025059.4:c.1877T>C MANE Select | NP_079335.2:p.Ile626Thr |