HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189062872C>A , CM000664.2:g.189062872C>A | GRCh38 |
NC_000002.11:g.189927598C>A , CM000664.1:g.189927598C>A | GRCh37 |
NC_000002.10:g.189635843C>A | NCBI36 |
NG_011799.1:g.122008G>T | |
NG_011799.2:g.122008G>T | |
NG_011799.3:g.167430G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374866.9:c.1970G>T MANE Select | ENSP00000364000.3:p.Gly657Val | |
ENST00000374866.7:c.1970G>T | ENSP00000364000.3:p.Gly657Val | |
ENST00000470524.2:n.76G>T | ||
ENST00000618828.1:c.809G>T | ENSP00000482184.1:p.Gly270Val | |
NM_000393.3:c.1970G>T | NP_000384.2:p.Gly657Val | |
XM_011510573.1:c.1832G>T | XP_011508875.1:p.Gly611Val | |
NM_000393.4:c.1970G>T | NP_000384.2:p.Gly657Val | |
XM_011510573.3:c.1832G>T | XP_011508875.1:p.Gly611Val | |
NM_000393.5:c.1970G>T MANE Select | NP_000384.2:p.Gly657Val |