Canonical Allele Identifier: CA28692561

Linked Data

dbSNP Id: rs535676824

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736727T>C , CM000663.2:g.109736727T>C GRCh38
NC_000001.10:g.110279349T>C , CM000663.1:g.110279349T>C GRCh37
NC_000001.9:g.110080872T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*344A>G (GSTM3) MANE Select ENSP00000354357.2:n.*344A>G
ENST00000256594.7:c.*344A>G (GSTM3) ENSP00000256594.3:n.*344A>G
ENST00000361066.6:c.*344A>G (GSTM3) ENSP00000354357.2:n.*344A>G
ENST00000429410.2:n.82+24379T>C (GSTM5)
NM_000849.4:c.*344A>G (GSTM3) NP_000840.2:n.*344A>G
NR_024537.1:n.1256A>G (GSTM3)
NM_000849.5:c.*344A>G (GSTM3) MANE Select NP_000840.2:n.*344A>G
NR_024537.2:n.1256A>G (GSTM3)