Canonical Allele Identifier: CA475395143
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591099677
MyVariant Identifiers: chr11:g.67352239C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584768C>G , CM000673.2:g.67584768C>G GRCh38
NC_000011.9:g.67352239C>G , CM000673.1:g.67352239C>G GRCh37
NC_000011.8:g.67108815C>G NCBI36
NG_012075.1:g.6174C>G , LRG_723:g.6174C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.228C>G ENSP00000381604.1:p.Thr76=
ENST00000398606.10:c.228C>G MANE Select ENSP00000381607.3:p.Thr76=
ENST00000646888.1:c.121C>G ENSP00000494477.1:p.Pro41Ala
ENST00000398603.5:c.228C>G ENSP00000381604.1:p.Thr76=
ENST00000398606.7:c.228C>G ENSP00000381607.3:p.Thr76=
ENST00000489040.1:n.227C>G
ENST00000494593.1:n.658C>G
ENST00000498765.5:c.191C>G
NM_000852.3:c.228C>G , LRG_723t1:c.228C>G NP_000843.1:p.Thr76=
NM_000852.4:c.228C>G MANE Select NP_000843.1:p.Thr76=
Search 100 bp 5'
Search 100 bp 3'