Canonical Allele Identifier: CA381516016
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352207T>A (hg19) chr11:g.67584736T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584736T>A , CM000673.2:g.67584736T>A GRCh38
NC_000011.9:g.67352207T>A , CM000673.1:g.67352207T>A GRCh37
NC_000011.8:g.67108783T>A NCBI36
NG_012075.1:g.6142T>A , LRG_723:g.6142T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.196T>A ENSP00000381604.1:p.Ser66Thr
ENST00000398606.10:c.196T>A MANE Select ENSP00000381607.3:p.Ser66Thr
ENST00000646888.1:c.89T>A ENSP00000494477.1:p.Val30Asp
ENST00000398603.5:c.196T>A ENSP00000381604.1:p.Ser66Thr
ENST00000398606.7:c.196T>A ENSP00000381607.3:p.Ser66Thr
ENST00000489040.1:n.195T>A
ENST00000494593.1:n.626T>A
ENST00000498765.5:c.159T>A
NM_000852.3:c.196T>A , LRG_723t1:c.196T>A NP_000843.1:p.Ser66Thr
NM_000852.4:c.196T>A MANE Select NP_000843.1:p.Ser66Thr
Search 100 bp 5'
Search 100 bp 3'