Canonical Allele Identifier: CA995122
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.109740350G>T
GRCh37 chr1:g.110282972G>T
gnomAD v2:
1:110282972 G / T
gnomAD v3:
1:109740350 G / T
gnomAD v4:
chr1-109740350-G-T
Joint Max Group AF 0.82702401 (AFR)
Genomes Max Group AF 0.82076222 (EAS)
Exomes Max Group AF 0.83046366 (AFR)
dbSNP:
1332018
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109740350G>T , CM000663.2:g.109740350G>T GRCh38
NC_000001.10:g.110282972G>T , CM000663.1:g.110282972G>T GRCh37
NC_000001.9:g.110084495G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.-63C>A (GSTM3) MANE Select ENSP00000354357.2:n.-63C>A
ENST00000256594.7:c.-63C>A (GSTM3) ENSP00000256594.3:n.-63C>A
ENST00000361066.6:c.-63C>A (GSTM3) ENSP00000354357.2:n.-63C>A
ENST00000429410.2:n.82+28002G>T (GSTM5)
NM_000849.4:c.-63C>A (GSTM3) NP_000840.2:n.-63C>A
NR_024537.1:n.248C>A (GSTM3)
XM_011541296.1:c.233C>A (GSTM3) XP_011539598.1:p.Ser78Ter
NM_000849.5:c.-63C>A (GSTM3) MANE Select NP_000840.2:n.-63C>A
NR_024537.2:n.248C>A (GSTM3)
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