Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10224511A= , CM000681.2:g.10224511A= | GRCh38 |
| NC_000019.9:g.10335187A= , CM000681.1:g.10335187A= | GRCh37 |
| NC_000019.8:g.10196187A= | NCBI36 |
| NG_028016.3:g.11776T= , LRG_362:g.11776T= | |
| NG_046802.1:g.12297T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646641.1:c.395T= (S1PR2) MANE Select | ENSP00000496438.1:p.Val132= | |
| ENST00000588952.5:c.-401-5642T= (DNMT1) | ENSP00000467050.1:n.-401-5642T= | |
| ENST00000590320.2:c.395T= (S1PR2) | ENSP00000466933.1:p.Val132= | |
| ENST00000592342.5:c.-284+6693T= (DNMT1) | ENSP00000465993.1:n.-284+6693T= | |
| NM_004230.3:c.395T= (S1PR2) | NP_004221.3:p.Val132= | |
| XM_011528425.1:c.395T= (S1PR2) | XP_011526727.1:p.Val132= | |
| NM_004230.4:c.395T= (S1PR2) MANE Select | NP_004221.3:p.Val132= |