Canonical Allele Identifier: CA475396547
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591100989
MyVariant Identifiers: chr11:g.67354021C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586550C>T , CM000673.2:g.67586550C>T GRCh38
NC_000011.9:g.67354021C>T , CM000673.1:g.67354021C>T GRCh37
NC_000011.8:g.67110597C>T NCBI36
NG_012075.1:g.7956C>T , LRG_723:g.7956C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.498C>T ENSP00000381604.1:p.Leu166=
ENST00000398606.10:c.606C>T MANE Select ENSP00000381607.3:p.Leu202=
ENST00000398603.5:c.498C>T ENSP00000381604.1:p.Leu166=
ENST00000398606.7:c.606C>T ENSP00000381607.3:p.Leu202=
ENST00000467591.1:n.717C>T
ENST00000494593.1:n.1578C>T
ENST00000498765.5:c.669C>T
NM_000852.3:c.606C>T , LRG_723t1:c.606C>T NP_000843.1:p.Leu202=
NM_000852.4:c.606C>T MANE Select NP_000843.1:p.Leu202=