Canonical Allele Identifier: CA475396259
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100779
MyVariant Identifiers: chr11:g.67353890T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586419T>C , CM000673.2:g.67586419T>C GRCh38
NC_000011.9:g.67353890T>C , CM000673.1:g.67353890T>C GRCh37
NC_000011.8:g.67110466T>C NCBI36
NG_012075.1:g.7825T>C , LRG_723:g.7825T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.367T>C ENSP00000381604.1:p.Leu123=
ENST00000398606.10:c.475T>C MANE Select ENSP00000381607.3:p.Leu159=
ENST00000646888.1:c.*191T>C ENSP00000494477.1:n.*191T>C
ENST00000398603.5:c.367T>C ENSP00000381604.1:p.Leu123=
ENST00000398606.7:c.475T>C ENSP00000381607.3:p.Leu159=
ENST00000467591.1:n.586T>C
ENST00000494593.1:n.1447T>C
ENST00000495996.1:c.201T>C ENSP00000484686.1:p.Thr67=
ENST00000498765.5:c.538T>C
NM_000852.3:c.475T>C , LRG_723t1:c.475T>C NP_000843.1:p.Leu159=
NM_000852.4:c.475T>C MANE Select NP_000843.1:p.Leu159=