Canonical Allele Identifier: CA381515646
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352178T>G (hg19) chr11:g.67584707T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584707T>G , CM000673.2:g.67584707T>G GRCh38
NC_000011.9:g.67352178T>G , CM000673.1:g.67352178T>G GRCh37
NC_000011.8:g.67108754T>G NCBI36
NG_012075.1:g.6113T>G , LRG_723:g.6113T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.167T>G ENSP00000381604.1:p.Phe56Cys
ENST00000398606.10:c.167T>G MANE Select ENSP00000381607.3:p.Phe56Cys
ENST00000646888.1:c.60T>G ENSP00000494477.1:p.Val20=
ENST00000398603.5:c.167T>G ENSP00000381604.1:p.Phe56Cys
ENST00000398606.7:c.167T>G ENSP00000381607.3:p.Phe56Cys
ENST00000489040.1:n.166T>G
ENST00000494593.1:n.597T>G
ENST00000498765.5:c.130T>G
NM_000852.3:c.167T>G , LRG_723t1:c.167T>G NP_000843.1:p.Phe56Cys
NM_000852.4:c.167T>G MANE Select NP_000843.1:p.Phe56Cys
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