Canonical Allele Identifier: CA679522611
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1256114731
MyVariant Identifiers: chr11:g.67353066G>A (hg19) chr11:g.67585595G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585595G>A , CM000673.2:g.67585595G>A GRCh38
NC_000011.9:g.67353066G>A , CM000673.1:g.67353066G>A GRCh37
NC_000011.8:g.67109642G>A NCBI36
NG_012075.1:g.7001G>A , LRG_723:g.7001G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+354G>A ENSP00000381604.1:n.336+354G>A
ENST00000398606.10:c.336+354G>A MANE Select ENSP00000381607.3:n.336+354G>A
ENST00000646888.1:c.*52+354G>A ENSP00000494477.1:n.*52+354G>A
ENST00000398603.5:c.336+354G>A ENSP00000381604.1:n.336+354G>A
ENST00000398606.7:c.336+354G>A ENSP00000381607.3:n.336+354G>A
ENST00000467591.1:n.447+354G>A
ENST00000494593.1:n.1131+354G>A
ENST00000498765.5:c.399+354G>A
NM_000852.3:c.336+354G>A , LRG_723t1:c.336+354G>A NP_000843.1:n.336+354G>A
NM_000852.4:c.336+354G>A MANE Select NP_000843.1:n.336+354G>A
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