Canonical Allele Identifier: CA419374475
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

gnomAD v4: 1-109737116-G-C
MyVariant Identifiers: chr1:g.110279738G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737116G>C , CM000663.2:g.109737116G>C GRCh38
NC_000001.10:g.110279738G>C , CM000663.1:g.110279738G>C GRCh37
NC_000001.9:g.110081261G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.633C>G (GSTM3) MANE Select ENSP00000354357.2:p.Pro211=
ENST00000256594.7:c.633C>G (GSTM3) ENSP00000256594.3:p.Pro211=
ENST00000361066.6:c.633C>G (GSTM3) ENSP00000354357.2:p.Pro211=
ENST00000429410.2:n.82+24768G>C (GSTM5)
ENST00000476321.5:n.601C>G (GSTM3)
ENST00000486823.5:n.597C>G (GSTM3)
ENST00000488824.1:n.978C>G (GSTM3)
NM_000849.4:c.633C>G (GSTM3) NP_000840.2:p.Pro211=
NR_024537.1:n.867C>G (GSTM3)
XM_011541296.1:c.852C>G (GSTM3) XP_011539598.1:p.Pro284=
NM_000849.5:c.633C>G (GSTM3) MANE Select NP_000840.2:p.Pro211=
NR_024537.2:n.867C>G (GSTM3)
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