Linked Data
dbSNP Id:
rs774388647
ExAC:
19:10335070 T / C
gnomAD v2:
19-10335070-T-C
gnomAD v4:
19-10224394-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10224394T>C , CM000681.2:g.10224394T>C | GRCh38 |
| NC_000019.9:g.10335070T>C , CM000681.1:g.10335070T>C | GRCh37 |
| NC_000019.8:g.10196070T>C | NCBI36 |
| NG_028016.3:g.11893A>G , LRG_362:g.11893A>G | |
| NG_046802.1:g.12414A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646641.1:c.512A>G (S1PR2) MANE Select | ENSP00000496438.1:p.Asn171Ser | |
| ENST00000588952.5:c.-401-5525A>G (DNMT1) | ENSP00000467050.1:n.-401-5525A>G | |
| ENST00000590320.2:c.512A>G (S1PR2) | ENSP00000466933.1:p.Asn171Ser | |
| ENST00000592342.5:c.-284+6810A>G (DNMT1) | ENSP00000465993.1:n.-284+6810A>G | |
| NM_004230.3:c.512A>G (S1PR2) | NP_004221.3:p.Asn171Ser | |
| XM_011528425.1:c.512A>G (S1PR2) | XP_011526727.1:p.Asn171Ser | |
| NM_004230.4:c.512A>G (S1PR2) MANE Select | NP_004221.3:p.Asn171Ser |