Canonical Allele Identifier: CA475395175
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352619G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585148G>A , CM000673.2:g.67585148G>A GRCh38
NC_000011.9:g.67352619G>A , CM000673.1:g.67352619G>A GRCh37
NC_000011.8:g.67109195G>A NCBI36
NG_012075.1:g.6554G>A , LRG_723:g.6554G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.243G>A ENSP00000381604.1:p.Gly81=
ENST00000398606.10:c.243G>A MANE Select ENSP00000381607.3:p.Gly81=
ENST00000646888.1:c.136G>A ENSP00000494477.1:p.Glu46Lys
ENST00000398603.5:c.243G>A ENSP00000381604.1:p.Gly81=
ENST00000398606.7:c.243G>A ENSP00000381607.3:p.Gly81=
ENST00000467591.1:n.354G>A
ENST00000494593.1:n.1038G>A
ENST00000498765.5:c.306G>A
NM_000852.3:c.243G>A , LRG_723t1:c.243G>A NP_000843.1:p.Gly81=
NM_000852.4:c.243G>A MANE Select NP_000843.1:p.Gly81=
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