Canonical Allele Identifier: CA341535620

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737109T>A , CM000663.2:g.109737109T>A GRCh38
NC_000001.10:g.110279731T>A , CM000663.1:g.110279731T>A GRCh37
NC_000001.9:g.110081254T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.640A>T (GSTM3) MANE Select ENSP00000354357.2:p.Asn214Tyr
ENST00000256594.7:c.640A>T (GSTM3) ENSP00000256594.3:p.Asn214Tyr
ENST00000361066.6:c.640A>T (GSTM3) ENSP00000354357.2:p.Asn214Tyr
ENST00000429410.2:n.82+24761T>A (GSTM5)
ENST00000476321.5:n.608A>T (GSTM3)
ENST00000486823.5:n.604A>T (GSTM3)
ENST00000488824.1:n.985A>T (GSTM3)
NM_000849.4:c.640A>T (GSTM3) NP_000840.2:p.Asn214Tyr
NR_024537.1:n.874A>T (GSTM3)
XM_011541296.1:c.859A>T (GSTM3) XP_011539598.1:p.Asn287Tyr
NM_000849.5:c.640A>T (GSTM3) MANE Select NP_000840.2:p.Asn214Tyr
NR_024537.2:n.874A>T (GSTM3)