Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94774453C>A , CM000672.2:g.94774453C>A | GRCh38 |
| NC_000010.10:g.96534210C>A , CM000672.1:g.96534210C>A | GRCh37 |
| NC_000010.9:g.96524200C>A | NCBI36 |
| NG_008384.2:g.16748C>A | |
| NG_008384.3:g.16773C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.169-605C>A (CYP2C19) MANE Select | ENSP00000360372.3:n.169-605C>A | |
| ENST00000645461.1:n.617C>A (CYP2C19) | ||
| ENST00000371321.7:c.169-605C>A (CYP2C19) | ENSP00000360372.3:n.169-605C>A | |
| ENST00000446659.1:n.181G>T (MTND4P19) | ||
| ENST00000464755.1:c.932-605C>A | ENSP00000483243.1:n.932-605C>A | |
| ENST00000480405.2:c.169-605C>A (CYP2C19) | ENSP00000483847.1:n.169-605C>A | |
| NM_000769.2:c.169-605C>A (CYP2C19) | NP_000760.1:n.169-605C>A | |
| NM_000769.4:c.169-605C>A (CYP2C19) MANE Select | NP_000760.1:n.169-605C>A |