Canonical Allele Identifier: CA341535740

Linked Data

dbSNP Id: rs1429656435

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737132T>G , CM000663.2:g.109737132T>G GRCh38
NC_000001.10:g.110279754T>G , CM000663.1:g.110279754T>G GRCh37
NC_000001.9:g.110081277T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.617A>C (GSTM3) MANE Select ENSP00000354357.2:p.Gln206Pro
ENST00000256594.7:c.617A>C (GSTM3) ENSP00000256594.3:p.Gln206Pro
ENST00000361066.6:c.617A>C (GSTM3) ENSP00000354357.2:p.Gln206Pro
ENST00000429410.2:n.82+24784T>G (GSTM5)
ENST00000476321.5:n.585A>C (GSTM3)
ENST00000486823.5:n.581A>C (GSTM3)
ENST00000488824.1:n.962A>C (GSTM3)
NM_000849.4:c.617A>C (GSTM3) NP_000840.2:p.Gln206Pro
NR_024537.1:n.851A>C (GSTM3)
XM_011541296.1:c.836A>C (GSTM3) XP_011539598.1:p.Gln279Pro
NM_000849.5:c.617A>C (GSTM3) MANE Select NP_000840.2:p.Gln206Pro
NR_024537.2:n.851A>C (GSTM3)