HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189058807C= , CM000664.2:g.189058807C= | GRCh38 |
NC_000002.11:g.189923533C= , CM000664.1:g.189923533C= | GRCh37 |
NC_000002.10:g.189631778C= | NCBI36 |
NG_011799.1:g.126073G= | |
NG_011799.2:g.126073G= | |
NG_011799.3:g.171495G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.2130+42G= MANE Select | ENSP00000364000.3:n.2130+42G= | |
ENST00000374866.7:c.2130+42G= | ENSP00000364000.3:n.2130+42G= | |
ENST00000470524.2:n.236+42G= | ||
ENST00000618828.1:c.969+42G= | ENSP00000482184.1:n.969+42G= | |
NM_000393.3:c.2130+42G= | NP_000384.2:n.2130+42G= | |
XM_011510573.1:c.1992+42G= | XP_011508875.1:n.1992+42G= | |
NM_000393.4:c.2130+42G= | NP_000384.2:n.2130+42G= | |
XM_011510573.3:c.1992+42G= | XP_011508875.1:n.1992+42G= | |
NM_000393.5:c.2130+42G= MANE Select | NP_000384.2:n.2130+42G= |