HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208129601C>G , CM000664.2:g.208129601C>G | GRCh38 |
NC_000002.11:g.208994325C>G , CM000664.1:g.208994325C>G | GRCh37 |
NC_000002.10:g.208702570C>G | NCBI36 |
NG_008038.1:g.5230G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282141.4:c.92G>C MANE Select | ENSP00000282141.3:p.Ser31Thr | |
ENST00000282141.3:c.92G>C | ENSP00000282141.3:p.Ser31Thr | |
NM_020989.3:c.92G>C | NP_066269.1:p.Ser31Thr | |
NR_038437.1:n.98-7455C>G | ||
XM_011510661.1:c.92G>C | XP_011508963.1:p.Ser31Thr | |
XM_011510662.1:c.92G>C | XP_011508964.1:p.Ser31Thr | |
XM_011510663.1:c.-38G>C | XP_011508965.1:n.-38G>C | |
NM_020989.4:c.92G>C MANE Select | NP_066269.1:p.Ser31Thr |