HGVS | Genome Assembly |
---|---|
NC_000001.11:g.109736882A>C , CM000663.2:g.109736882A>C | GRCh38 |
NC_000001.10:g.110279504A>C , CM000663.1:g.110279504A>C | GRCh37 |
NC_000001.9:g.110081027A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361066.7:c.*189T>G (GSTM3) MANE Select | ENSP00000354357.2:n.*189T>G | |
ENST00000256594.7:c.*189T>G (GSTM3) | ENSP00000256594.3:n.*189T>G | |
ENST00000361066.6:c.*189T>G (GSTM3) | ENSP00000354357.2:n.*189T>G | |
ENST00000429410.2:n.82+24534A>C (GSTM5) | ||
NM_000849.4:c.*189T>G (GSTM3) | NP_000840.2:n.*189T>G | |
NR_024537.1:n.1101T>G (GSTM3) | ||
NM_000849.5:c.*189T>G (GSTM3) MANE Select | NP_000840.2:n.*189T>G | |
NR_024537.2:n.1101T>G (GSTM3) |