Canonical Allele Identifier: CA994825

Linked Data

dbSNP Id: rs769305502

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737107G>T , CM000663.2:g.109737107G>T GRCh38
NC_000001.10:g.110279729G>T , CM000663.1:g.110279729G>T GRCh37
NC_000001.9:g.110081252G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.642C>A (GSTM3) MANE Select ENSP00000354357.2:p.Asn214Lys
ENST00000256594.7:c.642C>A (GSTM3) ENSP00000256594.3:p.Asn214Lys
ENST00000361066.6:c.642C>A (GSTM3) ENSP00000354357.2:p.Asn214Lys
ENST00000429410.2:n.82+24759G>T (GSTM5)
ENST00000476321.5:n.610C>A (GSTM3)
ENST00000486823.5:n.606C>A (GSTM3)
ENST00000488824.1:n.987C>A (GSTM3)
NM_000849.4:c.642C>A (GSTM3) NP_000840.2:p.Asn214Lys
NR_024537.1:n.876C>A (GSTM3)
XM_011541296.1:c.861C>A (GSTM3) XP_011539598.1:p.Asn287Lys
NM_000849.5:c.642C>A (GSTM3) MANE Select NP_000840.2:p.Asn214Lys
NR_024537.2:n.876C>A (GSTM3)