Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128259807C>G , CM000667.2:g.128259807C>G | GRCh38 |
| NC_000005.9:g.127595499C>G , CM000667.1:g.127595499C>G | GRCh37 |
| NC_000005.8:g.127623398C>G | NCBI36 |
| NG_008750.1:g.283237G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.8387G>C MANE Select | ENSP00000262464.4:p.Ser2796Thr | |
| ENST00000262464.8:c.8387G>C | ENSP00000262464.4:p.Ser2796Thr | |
| ENST00000508053.5:c.8387G>C | ENSP00000424571.1:p.Ser2796Thr | |
| ENST00000619499.4:c.8384G>C | ENSP00000482132.1:p.Ser2795Thr | |
| NM_001999.3:c.8387G>C | NP_001990.2:p.Ser2796Thr | |
| XM_017009228.2:c.8234G>C | XP_016864717.1:p.Ser2745Thr | |
| NM_001999.4:c.8387G>C MANE Select | NP_001990.2:p.Ser2796Thr |