HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780513C>A , CM000672.2:g.94780513C>A | GRCh38 |
NC_000010.10:g.96540270C>A , CM000672.1:g.96540270C>A | GRCh37 |
NC_000010.9:g.96530260C>A | NCBI36 |
NG_008384.2:g.22808C>A | |
NG_008384.3:g.22833C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.496C>A MANE Select | ENSP00000360372.3:p.Pro166Thr | |
ENST00000645461.1:n.1549C>A | ||
ENST00000371321.7:c.496C>A | ENSP00000360372.3:p.Pro166Thr | |
ENST00000464755.1:c.1259C>A | ENSP00000483243.1:n.1259C>A | |
NM_000769.2:c.496C>A | NP_000760.1:p.Pro166Thr | |
NM_000769.4:c.496C>A MANE Select | NP_000760.1:p.Pro166Thr |