HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189050745A>C , CM000664.2:g.189050745A>C | GRCh38 |
NC_000002.11:g.189915471A>C , CM000664.1:g.189915471A>C | GRCh37 |
NC_000002.10:g.189623716A>C | NCBI36 |
NG_011799.1:g.134135T>G | |
NG_011799.2:g.134135T>G | |
NG_011799.3:g.179557T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.2932-69T>G MANE Select | ENSP00000364000.3:n.2932-69T>G | |
ENST00000374866.7:c.2932-69T>G | ENSP00000364000.3:n.2932-69T>G | |
ENST00000618828.1:c.1771-69T>G | ENSP00000482184.1:n.1771-69T>G | |
NM_000393.3:c.2932-69T>G | NP_000384.2:n.2932-69T>G | |
XM_011510573.1:c.2794-69T>G | XP_011508875.1:n.2794-69T>G | |
NM_000393.4:c.2932-69T>G | NP_000384.2:n.2932-69T>G | |
XM_011510573.3:c.2794-69T>G | XP_011508875.1:n.2794-69T>G | |
NM_000393.5:c.2932-69T>G MANE Select | NP_000384.2:n.2932-69T>G |