Canonical Allele Identifier: CA2745006138

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109734282C>T , CM000663.2:g.109734282C>T GRCh38
NC_000001.10:g.110276904C>T , CM000663.1:g.110276904C>T GRCh37
NC_000001.9:g.110078427C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.*2789G>A (GSTM3) MANE Select ENSP00000354357.2:n.*2789G>A
ENST00000256594.7:c.*2789G>A (GSTM3) ENSP00000256594.3:n.*2789G>A
ENST00000429410.2:n.82+21934C>T (GSTM5)
NM_000849.4:c.*2789G>A (GSTM3) NP_000840.2:n.*2789G>A
NR_024537.1:n.3701G>A (GSTM3)
NM_000849.5:c.*2789G>A (GSTM3) MANE Select NP_000840.2:n.*2789G>A
NR_024537.2:n.3701G>A (GSTM3)