Linked Data
gnomAD v4:
19-10223804-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10223804A>C , CM000681.2:g.10223804A>C | GRCh38 |
| NC_000019.9:g.10334480A>C , CM000681.1:g.10334480A>C | GRCh37 |
| NC_000019.8:g.10195480A>C | NCBI36 |
| NG_028016.3:g.12483T>G , LRG_362:g.12483T>G | |
| NG_046802.1:g.13004T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646641.1:c.*40T>G (S1PR2) MANE Select | ENSP00000496438.1:n.*40T>G | |
| ENST00000588952.5:c.-401-4935T>G (DNMT1) | ENSP00000467050.1:n.-401-4935T>G | |
| ENST00000590320.2:c.*40T>G (S1PR2) | ENSP00000466933.1:n.*40T>G | |
| ENST00000592342.5:c.-284+7400T>G (DNMT1) | ENSP00000465993.1:n.-284+7400T>G | |
| NM_004230.3:c.*40T>G (S1PR2) | NP_004221.3:n.*40T>G | |
| XM_011528425.1:c.894+208T>G (S1PR2) | XP_011526727.1:n.894+208T>G | |
| NM_004230.4:c.*40T>G (S1PR2) MANE Select | NP_004221.3:n.*40T>G |