HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109736940C>A , CM000663.2:g.109736940C>A | GRCh38 |
NC_000001.10:g.110279562C>A , CM000663.1:g.110279562C>A | GRCh37 |
NC_000001.9:g.110081085C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361066.7:c.*131G>T (GSTM3) MANE Select | ENSP00000354357.2:n.*131G>T | |
ENST00000256594.7:c.*131G>T (GSTM3) | ENSP00000256594.3:n.*131G>T | |
ENST00000361066.6:c.*131G>T (GSTM3) | ENSP00000354357.2:n.*131G>T | |
ENST00000429410.2:n.82+24592C>A (GSTM5) | ||
ENST00000486823.5:n.773G>T (GSTM3) | ||
NM_000849.4:c.*131G>T (GSTM3) | NP_000840.2:n.*131G>T | |
NR_024537.1:n.1043G>T (GSTM3) | ||
NM_000849.5:c.*131G>T (GSTM3) MANE Select | NP_000840.2:n.*131G>T | |
NR_024537.2:n.1043G>T (GSTM3) |