Canonical Allele Identifier: CA28691339
Gene: GSTM3 HGNC NCBI
GSTM5 HGNC NCBI

Linked Data

dbSNP Id: rs552539495
gnomAD v3: 1-109734139-C-T
gnomAD v4: 1-109734139-C-T
MyVariant Identifiers: chr1:g.110276761C>T (hg19) chr1:g.109734139C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109734139C>T , CM000663.2:g.109734139C>T GRCh38
NC_000001.10:g.110276761C>T , CM000663.1:g.110276761C>T GRCh37
NC_000001.9:g.110078284C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.*2932G>A (GSTM3) MANE Select ENSP00000354357.2:n.*2932G>A
ENST00000256594.7:c.*2932G>A (GSTM3) ENSP00000256594.3:n.*2932G>A
ENST00000429410.2:n.82+21791C>T (GSTM5)
NM_000849.4:c.*2932G>A (GSTM3) NP_000840.2:n.*2932G>A
NR_024537.1:n.3844G>A (GSTM3)
NM_000849.5:c.*2932G>A (GSTM3) MANE Select NP_000840.2:n.*2932G>A
NR_024537.2:n.3844G>A (GSTM3)
Search 100 bp 5'
Search 100 bp 3'