Canonical Allele Identifier: CA419374292

Linked Data

MyVariant Identifiers: chr1:g.110279642C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737020C>A , CM000663.2:g.109737020C>A GRCh38
NC_000001.10:g.110279642C>A , CM000663.1:g.110279642C>A GRCh37
NC_000001.9:g.110081165C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*51G>T (GSTM3) MANE Select ENSP00000354357.2:n.*51G>T
ENST00000256594.7:c.*51G>T (GSTM3) ENSP00000256594.3:n.*51G>T
ENST00000361066.6:c.*51G>T (GSTM3) ENSP00000354357.2:n.*51G>T
ENST00000429410.2:n.82+24672C>A (GSTM5)
ENST00000476321.5:n.697G>T (GSTM3)
ENST00000486823.5:n.693G>T (GSTM3)
ENST00000488824.1:n.1074G>T (GSTM3)
NM_000849.4:c.*51G>T (GSTM3) NP_000840.2:n.*51G>T
NR_024537.1:n.963G>T (GSTM3)
XM_011541296.1:c.*51G>T (GSTM3) XP_011539598.1:n.*51G>T
NM_000849.5:c.*51G>T (GSTM3) MANE Select NP_000840.2:n.*51G>T
NR_024537.2:n.963G>T (GSTM3)