HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109736776C= , CM000663.2:g.109736776C= | GRCh38 |
NC_000001.10:g.110279398C= , CM000663.1:g.110279398C= | GRCh37 |
NC_000001.9:g.110080921C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361066.7:c.*295G= (GSTM3) MANE Select | ENSP00000354357.2:n.*295G= | |
ENST00000256594.7:c.*295G= (GSTM3) | ENSP00000256594.3:n.*295G= | |
ENST00000361066.6:c.*295G= (GSTM3) | ENSP00000354357.2:n.*295G= | |
ENST00000429410.2:n.82+24428C= (GSTM5) | ||
NM_000849.4:c.*295G= (GSTM3) | NP_000840.2:n.*295G= | |
NR_024537.1:n.1207G= (GSTM3) | ||
NM_000849.5:c.*295G= (GSTM3) MANE Select | NP_000840.2:n.*295G= | |
NR_024537.2:n.1207G= (GSTM3) |