HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109736959C>T , CM000663.2:g.109736959C>T | GRCh38 |
NC_000001.10:g.110279581C>T , CM000663.1:g.110279581C>T | GRCh37 |
NC_000001.9:g.110081104C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361066.7:c.*112G>A (GSTM3) MANE Select | ENSP00000354357.2:n.*112G>A | |
ENST00000256594.7:c.*112G>A (GSTM3) | ENSP00000256594.3:n.*112G>A | |
ENST00000361066.6:c.*112G>A (GSTM3) | ENSP00000354357.2:n.*112G>A | |
ENST00000429410.2:n.82+24611C>T (GSTM5) | ||
ENST00000486823.5:n.754G>A (GSTM3) | ||
NM_000849.4:c.*112G>A (GSTM3) | NP_000840.2:n.*112G>A | |
NR_024537.1:n.1024G>A (GSTM3) | ||
NM_000849.5:c.*112G>A (GSTM3) MANE Select | NP_000840.2:n.*112G>A | |
NR_024537.2:n.1024G>A (GSTM3) |