HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94774519T>G , CM000672.2:g.94774519T>G | GRCh38 |
NC_000010.10:g.96534276T>G , CM000672.1:g.96534276T>G | GRCh37 |
NC_000010.9:g.96524266T>G | NCBI36 |
NG_008384.2:g.16814T>G | |
NG_008384.3:g.16839T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.169-539T>G (CYP2C19) MANE Select | ENSP00000360372.3:n.169-539T>G | |
ENST00000645461.1:n.683T>G (CYP2C19) | ||
ENST00000371321.7:c.169-539T>G (CYP2C19) | ENSP00000360372.3:n.169-539T>G | |
ENST00000446659.1:n.115A>C (MTND4P19) | ||
ENST00000464755.1:c.932-539T>G | ENSP00000483243.1:n.932-539T>G | |
ENST00000480405.2:c.169-539T>G (CYP2C19) | ENSP00000483847.1:n.169-539T>G | |
NM_000769.2:c.169-539T>G (CYP2C19) | NP_000760.1:n.169-539T>G | |
NM_000769.4:c.169-539T>G (CYP2C19) MANE Select | NP_000760.1:n.169-539T>G |