Canonical Allele Identifier: CA994821

Gene: GSTM3 GSTM5

Linked Data

• dbSNP Id: rs770992867
• ExAC: 1:110279709 T / C
• gnomAD v2: 1-110279709-T-C
• gnomAD v3: 1-109737087-T-C
• gnomAD v4: 1-109737087-T-C
• MyVariant Identifiers: chr1:g.110279709T>C (hg19) ; chr1:g.109737087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737087T>C , CM000663.2:g.109737087T>C	GRCh38
NC_000001.10:g.110279709T>C , CM000663.1:g.110279709T>C	GRCh37
NC_000001.9:g.110081232T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361066.7:c.662A>G (GSTM3) MANE Select	ENSP00000354357.2:p.Asn221Ser
ENST00000256594.7:c.662A>G (GSTM3)	ENSP00000256594.3:p.Asn221Ser
ENST00000361066.6:c.662A>G (GSTM3)	ENSP00000354357.2:p.Asn221Ser
ENST00000429410.2:n.82+24739T>C (GSTM5)
ENST00000476321.5:n.630A>G (GSTM3)
ENST00000486823.5:n.626A>G (GSTM3)
ENST00000488824.1:n.1007A>G (GSTM3)
NM_000849.4:c.662A>G (GSTM3)	NP_000840.2:p.Asn221Ser
NR_024537.1:n.896A>G (GSTM3)
XM_011541296.1:c.881A>G (GSTM3)	XP_011539598.1:p.Asn294Ser
NM_000849.5:c.662A>G (GSTM3) MANE Select	NP_000840.2:p.Asn221Ser
NR_024537.2:n.896A>G (GSTM3)