HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94781957C= , CM000672.2:g.94781957C= | GRCh38 |
NC_000010.10:g.96541714C= , CM000672.1:g.96541714C= | GRCh37 |
NC_000010.9:g.96531704C= | NCBI36 |
NG_008384.2:g.24252C= | |
NG_008384.3:g.24277C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.779C= MANE Select | ENSP00000360372.3:p.Pro260= | |
ENST00000645461.1:n.1832C= | ||
ENST00000371321.7:c.779C= | ENSP00000360372.3:p.Pro260= | |
ENST00000464755.1:c.1542C= | ENSP00000483243.1:n.1542C= | |
NM_000769.2:c.779C= | NP_000760.1:p.Pro260= | |
NM_000769.4:c.779C= MANE Select | NP_000760.1:p.Pro260= |