Canonical Allele Identifier: CA419374510

Linked Data

MyVariant Identifiers: chr1:g.110279774A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737152A>C , CM000663.2:g.109737152A>C GRCh38
NC_000001.10:g.110279774A>C , CM000663.1:g.110279774A>C GRCh37
NC_000001.9:g.110081297A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.597T>G (GSTM3) MANE Select ENSP00000354357.2:p.Ala199=
ENST00000256594.7:c.597T>G (GSTM3) ENSP00000256594.3:p.Ala199=
ENST00000361066.6:c.597T>G (GSTM3) ENSP00000354357.2:p.Ala199=
ENST00000429410.2:n.82+24804A>C (GSTM5)
ENST00000476321.5:n.565T>G (GSTM3)
ENST00000486823.5:n.561T>G (GSTM3)
ENST00000488824.1:n.942T>G (GSTM3)
NM_000849.4:c.597T>G (GSTM3) NP_000840.2:p.Ala199=
NR_024537.1:n.831T>G (GSTM3)
XM_011541296.1:c.816T>G (GSTM3) XP_011539598.1:p.Ala272=
NM_000849.5:c.597T>G (GSTM3) MANE Select NP_000840.2:p.Ala199=
NR_024537.2:n.831T>G (GSTM3)