Canonical Allele Identifier: CA1188220349

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736772A= , CM000663.2:g.109736772A= GRCh38
NC_000001.10:g.110279394A= , CM000663.1:g.110279394A= GRCh37
NC_000001.9:g.110080917A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*299T= (GSTM3) MANE Select ENSP00000354357.2:n.*299T=
ENST00000256594.7:c.*299T= (GSTM3) ENSP00000256594.3:n.*299T=
ENST00000361066.6:c.*299T= (GSTM3) ENSP00000354357.2:n.*299T=
ENST00000429410.2:n.82+24424A= (GSTM5)
NM_000849.4:c.*299T= (GSTM3) NP_000840.2:n.*299T=
NR_024537.1:n.1211T= (GSTM3)
NM_000849.5:c.*299T= (GSTM3) MANE Select NP_000840.2:n.*299T=
NR_024537.2:n.1211T= (GSTM3)