HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189062888G>C , CM000664.2:g.189062888G>C | GRCh38 |
NC_000002.11:g.189927614G>C , CM000664.1:g.189927614G>C | GRCh37 |
NC_000002.10:g.189635859G>C | NCBI36 |
NG_011799.1:g.121992C>G | |
NG_011799.2:g.121992C>G | |
NG_011799.3:g.167414C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.1954C>G MANE Select | ENSP00000364000.3:p.Pro652Ala | |
ENST00000374866.7:c.1954C>G | ENSP00000364000.3:p.Pro652Ala | |
ENST00000470524.2:n.60C>G | ||
ENST00000618828.1:c.793C>G | ENSP00000482184.1:p.Pro265Ala | |
NM_000393.3:c.1954C>G | NP_000384.2:p.Pro652Ala | |
XM_011510573.1:c.1816C>G | XP_011508875.1:p.Pro606Ala | |
NM_000393.4:c.1954C>G | NP_000384.2:p.Pro652Ala | |
XM_011510573.3:c.1816C>G | XP_011508875.1:p.Pro606Ala | |
NM_000393.5:c.1954C>G MANE Select | NP_000384.2:p.Pro652Ala |