HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94774476T>C , CM000672.2:g.94774476T>C | GRCh38 |
NC_000010.10:g.96534233T>C , CM000672.1:g.96534233T>C | GRCh37 |
NC_000010.9:g.96524223T>C | NCBI36 |
NG_008384.2:g.16771T>C | |
NG_008384.3:g.16796T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.169-582T>C (CYP2C19) MANE Select | ENSP00000360372.3:n.169-582T>C | |
ENST00000645461.1:n.640T>C (CYP2C19) | ||
ENST00000371321.7:c.169-582T>C (CYP2C19) | ENSP00000360372.3:n.169-582T>C | |
ENST00000446659.1:n.158A>G (MTND4P19) | ||
ENST00000464755.1:c.932-582T>C | ENSP00000483243.1:n.932-582T>C | |
ENST00000480405.2:c.169-582T>C (CYP2C19) | ENSP00000483847.1:n.169-582T>C | |
NM_000769.2:c.169-582T>C (CYP2C19) | NP_000760.1:n.169-582T>C | |
NM_000769.4:c.169-582T>C (CYP2C19) MANE Select | NP_000760.1:n.169-582T>C |