Canonical Allele Identifier: CA419374190

Linked Data

MyVariant Identifiers: chr1:g.110279606T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736984T>G , CM000663.2:g.109736984T>G GRCh38
NC_000001.10:g.110279606T>G , CM000663.1:g.110279606T>G GRCh37
NC_000001.9:g.110081129T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*87A>C (GSTM3) MANE Select ENSP00000354357.2:n.*87A>C
ENST00000256594.7:c.*87A>C (GSTM3) ENSP00000256594.3:n.*87A>C
ENST00000361066.6:c.*87A>C (GSTM3) ENSP00000354357.2:n.*87A>C
ENST00000429410.2:n.82+24636T>G (GSTM5)
ENST00000476321.5:n.733A>C (GSTM3)
ENST00000486823.5:n.729A>C (GSTM3)
ENST00000488824.1:n.1110A>C (GSTM3)
NM_000849.4:c.*87A>C (GSTM3) NP_000840.2:n.*87A>C
NR_024537.1:n.999A>C (GSTM3)
XM_011541296.1:c.*87A>C (GSTM3) XP_011539598.1:n.*87A>C
NM_000849.5:c.*87A>C (GSTM3) MANE Select NP_000840.2:n.*87A>C
NR_024537.2:n.999A>C (GSTM3)