HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189062875A>G , CM000664.2:g.189062875A>G | GRCh38 |
NC_000002.11:g.189927601A>G , CM000664.1:g.189927601A>G | GRCh37 |
NC_000002.10:g.189635846A>G | NCBI36 |
NG_011799.1:g.122005T>C | |
NG_011799.2:g.122005T>C | |
NG_011799.3:g.167427T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374866.9:c.1967T>C MANE Select | ENSP00000364000.3:p.Val656Ala | |
ENST00000374866.7:c.1967T>C | ENSP00000364000.3:p.Val656Ala | |
ENST00000470524.2:n.73T>C | ||
ENST00000618828.1:c.806T>C | ENSP00000482184.1:p.Val269Ala | |
NM_000393.3:c.1967T>C | NP_000384.2:p.Val656Ala | |
XM_011510573.1:c.1829T>C | XP_011508875.1:p.Val610Ala | |
NM_000393.4:c.1967T>C | NP_000384.2:p.Val656Ala | |
XM_011510573.3:c.1829T>C | XP_011508875.1:p.Val610Ala | |
NM_000393.5:c.1967T>C MANE Select | NP_000384.2:p.Val656Ala |