Canonical Allele Identifier: CA28692792

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs541685561
• gnomAD v2: 1-110279880-G-A
• gnomAD v3: 1-109737258-G-A
• gnomAD v4: 1-109737258-G-A
• MyVariant Identifiers: chr1:g.110279880G>A (hg19) ; chr1:g.109737258G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737258G>A , CM000663.2:g.109737258G>A	GRCh38
NC_000001.10:g.110279880G>A , CM000663.1:g.110279880G>A	GRCh37
NC_000001.9:g.110081403G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.580-89C>T (GSTM3) MANE Select	ENSP00000354357.2:n.580-89C>T
ENST00000256594.7:c.580-89C>T (GSTM3)	ENSP00000256594.3:n.580-89C>T
ENST00000361066.6:c.580-89C>T (GSTM3)	ENSP00000354357.2:n.580-89C>T
ENST00000429410.2:n.82+24910G>A (GSTM5)
ENST00000476321.5:n.459C>T (GSTM3)
ENST00000486823.5:n.544-89C>T (GSTM3)
ENST00000488824.1:n.925-89C>T (GSTM3)
NM_000849.4:c.580-89C>T (GSTM3)	NP_000840.2:n.580-89C>T
NR_024537.1:n.814-89C>T (GSTM3)
XM_011541296.1:c.799-89C>T (GSTM3)	XP_011539598.1:n.799-89C>T
NM_000849.5:c.580-89C>T (GSTM3) MANE Select	NP_000840.2:n.580-89C>T
NR_024537.2:n.814-89C>T (GSTM3)