Canonical Allele Identifier: CA381519968
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs770460061
gnomAD v2: 11-67352710-T-C
gnomAD v4: 11-67585239-T-C
MyVariant Identifiers: chr11:g.67352710T>C (hg19) chr11:g.67585239T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585239T>C , CM000673.2:g.67585239T>C GRCh38
NC_000011.9:g.67352710T>C , CM000673.1:g.67352710T>C GRCh37
NC_000011.8:g.67109286T>C NCBI36
NG_012075.1:g.6645T>C , LRG_723:g.6645T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.334T>C ENSP00000381604.1:p.Tyr112His
ENST00000398606.10:c.334T>C MANE Select ENSP00000381607.3:p.Tyr112His
ENST00000646888.1:c.*50T>C ENSP00000494477.1:n.*50T>C
ENST00000398603.5:c.334T>C ENSP00000381604.1:p.Tyr112His
ENST00000398606.7:c.334T>C ENSP00000381607.3:p.Tyr112His
ENST00000467591.1:n.445T>C
ENST00000494593.1:n.1129T>C
ENST00000498765.5:c.397T>C
NM_000852.3:c.334T>C , LRG_723t1:c.334T>C NP_000843.1:p.Tyr112His
NM_000852.4:c.334T>C MANE Select NP_000843.1:p.Tyr112His
Search 100 bp 5'
Search 100 bp 3'