Canonical Allele Identifier: CA6142916
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs538776740
ExAC: 11:67354012 C / T
gnomAD v2: 11-67354012-C-T
gnomAD v3: 11-67586541-C-T
gnomAD v4: 11-67586541-C-T
COSMIC: COSM931133
MyVariant Identifiers: chr11:g.67354012C>T (hg19) chr11:g.67586541C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586541C>T , CM000673.2:g.67586541C>T GRCh38
NC_000011.9:g.67354012C>T , CM000673.1:g.67354012C>T GRCh37
NC_000011.8:g.67110588C>T NCBI36
NG_012075.1:g.7947C>T , LRG_723:g.7947C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.489C>T ENSP00000381604.1:p.Tyr163=
ENST00000398606.10:c.597C>T MANE Select ENSP00000381607.3:p.Tyr199=
ENST00000398603.5:c.489C>T ENSP00000381604.1:p.Tyr163=
ENST00000398606.7:c.597C>T ENSP00000381607.3:p.Tyr199=
ENST00000467591.1:n.708C>T
ENST00000494593.1:n.1569C>T
ENST00000498765.5:c.660C>T
NM_000852.3:c.597C>T , LRG_723t1:c.597C>T NP_000843.1:p.Tyr199=
NM_000852.4:c.597C>T MANE Select NP_000843.1:p.Tyr199=
Search 100 bp 5'
Search 100 bp 3'