Linked Data
dbSNP Id:
rs10211
gnomAD v3:
7-99705371-T-C
gnomAD v4:
7-99705371-T-C
MyVariant Identifiers:
chr7:g.99705371T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.99705371T>C , CM000669.2:g.99705371T>C | GRCh38 |
| NG_007983.1:g.34828A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000336374.4:c.*129A>G (CYP3A7) MANE Select | ENSP00000337450.2:n.*129A>G | |
| ENST00000620220.6:c.1416+2441A>G (CYP3A7-CYP3A51P) | ENSP00000479282.3:n.1416+2441A>G | |
| ENST00000336374.3:c.*129A>G (CYP3A7) | ENSP00000337450.2:n.*129A>G | |
| ENST00000477357.5:n.1980A>G (CYP3A7) | ||
| ENST00000611620.4:c.1497+144A>G (CYP3A7-CYP3A51P) | ENSP00000480571.1:n.1497+144A>G | |
| ENST00000620220.4:c.1416+2441A>G (CYP3A7-CYP3A51P) | ENSP00000479282.1:n.1416+2441A>G | |
| NM_000765.4:c.*129A>G (CYP3A7) | NP_000756.3:n.*129A>G | |
| NM_001256497.2:c.1497+144A>G (CYP3A7-CYP3A51P) | NP_001243426.2:n.1497+144A>G | |
| XR_927402.1:n.1467-18104T>C (ZSCAN25) | ||
| XR_927402.2:n.1466-18104T>C (ZSCAN25) | ||
| NM_000765.5:c.*129A>G (CYP3A7) MANE Select | NP_000756.3:n.*129A>G | |
| NM_001256497.3:c.1497+144A>G (CYP3A7-CYP3A51P) | NP_001243426.2:n.1497+144A>G |