Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.16326748C>G , CM000668.2:g.16326748C>G | GRCh38 |
| NC_000006.11:g.16326979C>G , CM000668.1:g.16326979C>G | GRCh37 |
| NC_000006.10:g.16434958C>G | NCBI36 |
| NG_011571.1:g.439743G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436367.6:c.1563G>C MANE Select | ENSP00000416360.1:p.Thr521= | |
| ENST00000244769.8:c.1563G>C | ENSP00000244769.3:p.Thr521= | |
| ENST00000436367.5:c.1563G>C | ENSP00000416360.1:p.Thr521= | |
| NM_000332.3:c.1563G>C | NP_000323.2:p.Thr521= | |
| NM_001128164.1:c.1563G>C | NP_001121636.1:p.Thr521= | |
| NM_001357857.1:c.*976G>C | NP_001344786.1:n.*976G>C | |
| NM_001357857.2:c.*976G>C | NP_001344786.1:n.*976G>C | |
| NM_001128164.2:c.1563G>C MANE Select | NP_001121636.1:p.Thr521= | |
| NM_000332.4:c.1563G>C | NP_000323.2:p.Thr521= |