Canonical Allele Identifier: CA6142742
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs377039913
ExAC: 11:67352197 C / T
gnomAD v2: 11-67352197-C-T
gnomAD v3: 11-67584726-C-T
gnomAD v4: 11-67584726-C-T
MyVariant Identifiers: chr11:g.67352197C>T (hg19) chr11:g.67584726C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584726C>T , CM000673.2:g.67584726C>T GRCh38
NC_000011.9:g.67352197C>T , CM000673.1:g.67352197C>T GRCh37
NC_000011.8:g.67108773C>T NCBI36
NG_012075.1:g.6132C>T , LRG_723:g.6132C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.186C>T ENSP00000381604.1:p.Thr62=
ENST00000398606.10:c.186C>T MANE Select ENSP00000381607.3:p.Thr62=
ENST00000646888.1:c.79C>T ENSP00000494477.1:p.Pro27Ser
ENST00000398603.5:c.186C>T ENSP00000381604.1:p.Thr62=
ENST00000398606.7:c.186C>T ENSP00000381607.3:p.Thr62=
ENST00000489040.1:n.185C>T
ENST00000494593.1:n.616C>T
ENST00000498765.5:c.149C>T
NM_000852.3:c.186C>T , LRG_723t1:c.186C>T NP_000843.1:p.Thr62=
NM_000852.4:c.186C>T MANE Select NP_000843.1:p.Thr62=
Search 100 bp 5'
Search 100 bp 3'