HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133528530G>C , CM000672.2:g.133528530G>C | GRCh38 |
NC_000010.10:g.135342034G>C , CM000672.1:g.135342034G>C | GRCh37 |
NC_000010.9:g.135192024G>C | NCBI36 |
NG_008383.1:g.6168G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.227G>C MANE Select | ENSP00000252945.3:p.Arg76Pro | |
ENST00000252945.7:c.227G>C | ENSP00000252945.3:p.Arg76Pro | |
ENST00000418356.1:c.76+958G>C | ENSP00000397299.1:n.76+958G>C | |
ENST00000421586.5:c.76+958G>C | ENSP00000412754.1:n.76+958G>C | |
ENST00000463117.6:c.227G>C | ENSP00000440689.1:p.Arg76Pro | |
ENST00000477500.5:n.188G>C | ||
ENST00000480558.1:n.452G>C | ||
ENST00000541080.5:c.76+958G>C | ||
ENST00000541261.1:c.227G>C | ENSP00000437799.1:p.Arg76Pro | |
NM_000773.3:c.227G>C | NP_000764.1:p.Arg76Pro | |
NM_000773.4:c.227G>C MANE Select | NP_000764.1:p.Arg76Pro |