Linked Data
dbSNP Id:
rs1168179043
gnomAD v2:
19-10335069-G-A
gnomAD v3:
19-10224393-G-A
gnomAD v4:
19-10224393-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10224393G>A , CM000681.2:g.10224393G>A | GRCh38 |
| NC_000019.9:g.10335069G>A , CM000681.1:g.10335069G>A | GRCh37 |
| NC_000019.8:g.10196069G>A | NCBI36 |
| NG_028016.3:g.11894C>T , LRG_362:g.11894C>T | |
| NG_046802.1:g.12415C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646641.1:c.513C>T (S1PR2) MANE Select | ENSP00000496438.1:p.Asn171= | |
| ENST00000588952.5:c.-401-5524C>T (DNMT1) | ENSP00000467050.1:n.-401-5524C>T | |
| ENST00000590320.2:c.513C>T (S1PR2) | ENSP00000466933.1:p.Asn171= | |
| ENST00000592342.5:c.-284+6811C>T (DNMT1) | ENSP00000465993.1:n.-284+6811C>T | |
| NM_004230.3:c.513C>T (S1PR2) | NP_004221.3:p.Asn171= | |
| XM_011528425.1:c.513C>T (S1PR2) | XP_011526727.1:p.Asn171= | |
| NM_004230.4:c.513C>T (S1PR2) MANE Select | NP_004221.3:p.Asn171= |