Canonical Allele Identifier: CA341535626

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737110G>C , CM000663.2:g.109737110G>C GRCh38
NC_000001.10:g.110279732G>C , CM000663.1:g.110279732G>C GRCh37
NC_000001.9:g.110081255G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.639C>G (GSTM3) MANE Select ENSP00000354357.2:p.Asn213Lys
ENST00000256594.7:c.639C>G (GSTM3) ENSP00000256594.3:p.Asn213Lys
ENST00000361066.6:c.639C>G (GSTM3) ENSP00000354357.2:p.Asn213Lys
ENST00000429410.2:n.82+24762G>C (GSTM5)
ENST00000476321.5:n.607C>G (GSTM3)
ENST00000486823.5:n.603C>G (GSTM3)
ENST00000488824.1:n.984C>G (GSTM3)
NM_000849.4:c.639C>G (GSTM3) NP_000840.2:p.Asn213Lys
NR_024537.1:n.873C>G (GSTM3)
XM_011541296.1:c.858C>G (GSTM3) XP_011539598.1:p.Asn286Lys
NM_000849.5:c.639C>G (GSTM3) MANE Select NP_000840.2:p.Asn213Lys
NR_024537.2:n.873C>G (GSTM3)