HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538809G>C , CM000672.2:g.133538809G>C | GRCh38 |
NC_000010.10:g.135352313G>C , CM000672.1:g.135352313G>C | GRCh37 |
NC_000010.9:g.135202303G>C | NCBI36 |
NG_008383.1:g.16447G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1327G>C MANE Select | ENSP00000252945.3:p.Ala443Pro | |
ENST00000252945.7:c.1327G>C | ENSP00000252945.3:p.Ala443Pro | |
ENST00000368520.1:n.1358+917G>C | ||
ENST00000418356.1:c.916G>C | ENSP00000397299.1:p.Ala306Pro | |
ENST00000421586.5:c.1066G>C | ENSP00000412754.1:p.Ala356Pro | |
ENST00000463117.6:c.1327G>C | ENSP00000440689.1:p.Ala443Pro | |
ENST00000469258.1:n.423G>C | ||
ENST00000541080.5:c.743G>C | ||
NM_000773.3:c.1327G>C | NP_000764.1:p.Ala443Pro | |
NM_000773.4:c.1327G>C MANE Select | NP_000764.1:p.Ala443Pro |