Canonical Allele Identifier: CA419374004

Linked Data

MyVariant Identifiers: chr1:g.110279575G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109736953G>A , CM000663.2:g.109736953G>A GRCh38
NC_000001.10:g.110279575G>A , CM000663.1:g.110279575G>A GRCh37
NC_000001.9:g.110081098G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361066.7:c.*118C>T (GSTM3) MANE Select ENSP00000354357.2:n.*118C>T
ENST00000256594.7:c.*118C>T (GSTM3) ENSP00000256594.3:n.*118C>T
ENST00000361066.6:c.*118C>T (GSTM3) ENSP00000354357.2:n.*118C>T
ENST00000429410.2:n.82+24605G>A (GSTM5)
ENST00000486823.5:n.760C>T (GSTM3)
NM_000849.4:c.*118C>T (GSTM3) NP_000840.2:n.*118C>T
NR_024537.1:n.1030C>T (GSTM3)
NM_000849.5:c.*118C>T (GSTM3) MANE Select NP_000840.2:n.*118C>T
NR_024537.2:n.1030C>T (GSTM3)