Canonical Allele Identifier: CA2646987386

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736882A>C , CM000663.2:g.109736882A>C GRCh38
NC_000001.10:g.110279504A>C , CM000663.1:g.110279504A>C GRCh37
NC_000001.9:g.110081027A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*189T>G (GSTM3) MANE Select ENSP00000354357.2:n.*189T>G
ENST00000256594.7:c.*189T>G (GSTM3) ENSP00000256594.3:n.*189T>G
ENST00000361066.6:c.*189T>G (GSTM3) ENSP00000354357.2:n.*189T>G
ENST00000429410.2:n.82+24534A>C (GSTM5)
NM_000849.4:c.*189T>G (GSTM3) NP_000840.2:n.*189T>G
NR_024537.1:n.1101T>G (GSTM3)
NM_000849.5:c.*189T>G (GSTM3) MANE Select NP_000840.2:n.*189T>G
NR_024537.2:n.1101T>G (GSTM3)