HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5689666A>C , CM000673.2:g.5689666A>C | GRCh38 |
NC_000011.9:g.5710896A>C , CM000673.1:g.5710896A>C | GRCh37 |
NC_000011.8:g.5667472A>C | NCBI36 |
NG_029122.1:g.444T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000460454.2:n.57A>C (TRIM22) | ||
ENST00000699052.1:n.4A>C (TRIM22) | ||
ENST00000380027.5:c.-440-4272T>G (TRIM5) | ENSP00000369366.1:n.-440-4272T>G | |
ENST00000412903.1:c.-61-9428T>G (TRIM5) | ENSP00000388031.1:n.-61-9428T>G | |
NM_001199573.1:c.-300A>C (TRIM22) | NP_001186502.1:n.-300A>C | |
NM_006074.4:c.-300A>C (TRIM22) | NP_006065.2:n.-300A>C |