Canonical Allele Identifier: CA2646984950

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109734140C>A , CM000663.2:g.109734140C>A GRCh38
NC_000001.10:g.110276762C>A , CM000663.1:g.110276762C>A GRCh37
NC_000001.9:g.110078285C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.*2931G>T (GSTM3) MANE Select ENSP00000354357.2:n.*2931G>T
ENST00000256594.7:c.*2931G>T (GSTM3) ENSP00000256594.3:n.*2931G>T
ENST00000429410.2:n.82+21792C>A (GSTM5)
NM_000849.4:c.*2931G>T (GSTM3) NP_000840.2:n.*2931G>T
NR_024537.1:n.3843G>T (GSTM3)
NM_000849.5:c.*2931G>T (GSTM3) MANE Select NP_000840.2:n.*2931G>T
NR_024537.2:n.3843G>T (GSTM3)