Canonical Allele Identifier: CA419374109

Linked Data

MyVariant Identifiers: chr1:g.110279583C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736961C>G , CM000663.2:g.109736961C>G GRCh38
NC_000001.10:g.110279583C>G , CM000663.1:g.110279583C>G GRCh37
NC_000001.9:g.110081106C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*110G>C (GSTM3) MANE Select ENSP00000354357.2:n.*110G>C
ENST00000256594.7:c.*110G>C (GSTM3) ENSP00000256594.3:n.*110G>C
ENST00000361066.6:c.*110G>C (GSTM3) ENSP00000354357.2:n.*110G>C
ENST00000429410.2:n.82+24613C>G (GSTM5)
ENST00000486823.5:n.752G>C (GSTM3)
NM_000849.4:c.*110G>C (GSTM3) NP_000840.2:n.*110G>C
NR_024537.1:n.1022G>C (GSTM3)
NM_000849.5:c.*110G>C (GSTM3) MANE Select NP_000840.2:n.*110G>C
NR_024537.2:n.1022G>C (GSTM3)