Canonical Allele Identifier: CA2646988108

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109737331T>C , CM000663.2:g.109737331T>C GRCh38
NC_000001.10:g.110279953T>C , CM000663.1:g.110279953T>C GRCh37
NC_000001.9:g.110081476T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.579+126A>G (GSTM3) MANE Select ENSP00000354357.2:n.579+126A>G
ENST00000256594.7:c.579+126A>G (GSTM3) ENSP00000256594.3:n.579+126A>G
ENST00000361066.6:c.579+126A>G (GSTM3) ENSP00000354357.2:n.579+126A>G
ENST00000429410.2:n.82+24983T>C (GSTM5)
ENST00000476321.5:n.386A>G (GSTM3)
ENST00000486823.5:n.543+126A>G (GSTM3)
ENST00000488824.1:n.924+126A>G (GSTM3)
NM_000849.4:c.579+126A>G (GSTM3) NP_000840.2:n.579+126A>G
NR_024537.1:n.813+126A>G (GSTM3)
XM_011541296.1:c.798+126A>G (GSTM3) XP_011539598.1:n.798+126A>G
NM_000849.5:c.579+126A>G (GSTM3) MANE Select NP_000840.2:n.579+126A>G
NR_024537.2:n.813+126A>G (GSTM3)