Canonical Allele Identifier: CA2646984952

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109734144G>T , CM000663.2:g.109734144G>T GRCh38
NC_000001.10:g.110276766G>T , CM000663.1:g.110276766G>T GRCh37
NC_000001.9:g.110078289G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361066.7:c.*2927C>A (GSTM3) MANE Select ENSP00000354357.2:n.*2927C>A
ENST00000256594.7:c.*2927C>A (GSTM3) ENSP00000256594.3:n.*2927C>A
ENST00000429410.2:n.82+21796G>T (GSTM5)
NM_000849.4:c.*2927C>A (GSTM3) NP_000840.2:n.*2927C>A
NR_024537.1:n.3839C>A (GSTM3)
NM_000849.5:c.*2927C>A (GSTM3) MANE Select NP_000840.2:n.*2927C>A
NR_024537.2:n.3839C>A (GSTM3)