Canonical Allele Identifier: CA419374443

Linked Data

MyVariant Identifiers: chr1:g.110279702A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737080A>T , CM000663.2:g.109737080A>T GRCh38
NC_000001.10:g.110279702A>T , CM000663.1:g.110279702A>T GRCh37
NC_000001.9:g.110081225A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.669T>A (GSTM3) MANE Select ENSP00000354357.2:p.Pro223=
ENST00000256594.7:c.669T>A (GSTM3) ENSP00000256594.3:p.Pro223=
ENST00000361066.6:c.669T>A (GSTM3) ENSP00000354357.2:p.Pro223=
ENST00000429410.2:n.82+24732A>T (GSTM5)
ENST00000476321.5:n.637T>A (GSTM3)
ENST00000486823.5:n.633T>A (GSTM3)
ENST00000488824.1:n.1014T>A (GSTM3)
NM_000849.4:c.669T>A (GSTM3) NP_000840.2:p.Pro223=
NR_024537.1:n.903T>A (GSTM3)
XM_011541296.1:c.888T>A (GSTM3) XP_011539598.1:p.Pro296=
NM_000849.5:c.669T>A (GSTM3) MANE Select NP_000840.2:p.Pro223=
NR_024537.2:n.903T>A (GSTM3)