Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10223842C= , CM000681.2:g.10223842C= | GRCh38 |
| NC_000019.9:g.10334518C= , CM000681.1:g.10334518C= | GRCh37 |
| NC_000019.8:g.10195518C= | NCBI36 |
| NG_028016.3:g.12445G= , LRG_362:g.12445G= | |
| NG_046802.1:g.12966G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646641.1:c.*2G= (S1PR2) MANE Select | ENSP00000496438.1:n.*2G= | |
| ENST00000588952.5:c.-401-4973G= (DNMT1) | ENSP00000467050.1:n.-401-4973G= | |
| ENST00000590320.2:c.*2G= (S1PR2) | ENSP00000466933.1:n.*2G= | |
| ENST00000592342.5:c.-284+7362G= (DNMT1) | ENSP00000465993.1:n.-284+7362G= | |
| NM_004230.3:c.*2G= (S1PR2) | NP_004221.3:n.*2G= | |
| XM_011528425.1:c.894+170G= (S1PR2) | XP_011526727.1:n.894+170G= | |
| NM_004230.4:c.*2G= (S1PR2) MANE Select | NP_004221.3:n.*2G= |