Canonical Allele Identifier: CA419374493

Linked Data

MyVariant Identifiers: chr1:g.110279759A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737137A>C , CM000663.2:g.109737137A>C GRCh38
NC_000001.10:g.110279759A>C , CM000663.1:g.110279759A>C GRCh37
NC_000001.9:g.110081282A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.612T>G (GSTM3) MANE Select ENSP00000354357.2:p.Ser204=
ENST00000256594.7:c.612T>G (GSTM3) ENSP00000256594.3:p.Ser204=
ENST00000361066.6:c.612T>G (GSTM3) ENSP00000354357.2:p.Ser204=
ENST00000429410.2:n.82+24789A>C (GSTM5)
ENST00000476321.5:n.580T>G (GSTM3)
ENST00000486823.5:n.576T>G (GSTM3)
ENST00000488824.1:n.957T>G (GSTM3)
NM_000849.4:c.612T>G (GSTM3) NP_000840.2:p.Ser204=
NR_024537.1:n.846T>G (GSTM3)
XM_011541296.1:c.831T>G (GSTM3) XP_011539598.1:p.Ser277=
NM_000849.5:c.612T>G (GSTM3) MANE Select NP_000840.2:p.Ser204=
NR_024537.2:n.846T>G (GSTM3)