Canonical Allele Identifier: CA419374141

Linked Data

MyVariant Identifiers: chr1:g.110279592A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736970A>T , CM000663.2:g.109736970A>T GRCh38
NC_000001.10:g.110279592A>T , CM000663.1:g.110279592A>T GRCh37
NC_000001.9:g.110081115A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*101T>A (GSTM3) MANE Select ENSP00000354357.2:n.*101T>A
ENST00000256594.7:c.*101T>A (GSTM3) ENSP00000256594.3:n.*101T>A
ENST00000361066.6:c.*101T>A (GSTM3) ENSP00000354357.2:n.*101T>A
ENST00000429410.2:n.82+24622A>T (GSTM5)
ENST00000486823.5:n.743T>A (GSTM3)
NM_000849.4:c.*101T>A (GSTM3) NP_000840.2:n.*101T>A
NR_024537.1:n.1013T>A (GSTM3)
XM_011541296.1:c.*101T>A (GSTM3) XP_011539598.1:n.*101T>A
NM_000849.5:c.*101T>A (GSTM3) MANE Select NP_000840.2:n.*101T>A
NR_024537.2:n.1013T>A (GSTM3)