HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189098758A>G , CM000664.2:g.189098758A>G | GRCh38 |
NC_000002.11:g.189963484A>G , CM000664.1:g.189963484A>G | GRCh37 |
NC_000002.10:g.189671729A>G | NCBI36 |
NG_011799.1:g.86122T>C | |
NG_011799.2:g.86122T>C | |
NG_011799.3:g.131544T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.371T>C MANE Select | ENSP00000364000.3:p.Val124Ala | |
ENST00000649966.1:c.233T>C | ENSP00000496785.1:p.Val78Ala | |
ENST00000374866.7:c.371T>C | ENSP00000364000.3:p.Val124Ala | |
ENST00000618828.1:c.-260T>C | ENSP00000482184.1:n.-260T>C | |
NM_000393.3:c.371T>C | NP_000384.2:p.Val124Ala | |
XM_011510573.1:c.233T>C | XP_011508875.1:p.Val78Ala | |
NM_000393.4:c.371T>C | NP_000384.2:p.Val124Ala | |
XM_011510573.3:c.233T>C | XP_011508875.1:p.Val78Ala | |
NM_000393.5:c.371T>C MANE Select | NP_000384.2:p.Val124Ala |