Linked Data
gnomAD v4:
19-10223912-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10223912T>C , CM000681.2:g.10223912T>C | GRCh38 |
| NC_000019.9:g.10334588T>C , CM000681.1:g.10334588T>C | GRCh37 |
| NC_000019.8:g.10195588T>C | NCBI36 |
| NG_028016.3:g.12375A>G , LRG_362:g.12375A>G | |
| NG_046802.1:g.12896A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646641.1:c.994A>G (S1PR2) MANE Select | ENSP00000496438.1:p.Ser332Gly | |
| ENST00000588952.5:c.-401-5043A>G (DNMT1) | ENSP00000467050.1:n.-401-5043A>G | |
| ENST00000590320.2:c.994A>G (S1PR2) | ENSP00000466933.1:p.Ser332Gly | |
| ENST00000592342.5:c.-284+7292A>G (DNMT1) | ENSP00000465993.1:n.-284+7292A>G | |
| NM_004230.3:c.994A>G (S1PR2) | NP_004221.3:p.Ser332Gly | |
| XM_011528425.1:c.894+100A>G (S1PR2) | XP_011526727.1:n.894+100A>G | |
| NM_004230.4:c.994A>G (S1PR2) MANE Select | NP_004221.3:p.Ser332Gly |