HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189062995A= , CM000664.2:g.189062995A= | GRCh38 |
NC_000002.11:g.189927721A= , CM000664.1:g.189927721A= | GRCh37 |
NC_000002.10:g.189635966A= | NCBI36 |
NG_011799.1:g.121885T= | |
NG_011799.2:g.121885T= | |
NG_011799.3:g.167307T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.1923+15T= MANE Select | ENSP00000364000.3:n.1923+15T= | |
ENST00000374866.7:c.1923+15T= | ENSP00000364000.3:n.1923+15T= | |
ENST00000470524.2:n.29+15T= | ||
ENST00000618828.1:c.762+15T= | ENSP00000482184.1:n.762+15T= | |
NM_000393.3:c.1923+15T= | NP_000384.2:n.1923+15T= | |
XM_011510573.1:c.1785+15T= | XP_011508875.1:n.1785+15T= | |
NM_000393.4:c.1923+15T= | NP_000384.2:n.1923+15T= | |
XM_011510573.3:c.1785+15T= | XP_011508875.1:n.1785+15T= | |
NM_000393.5:c.1923+15T= MANE Select | NP_000384.2:n.1923+15T= |