Canonical Allele Identifier: CA475394668
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352197C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584726C>G , CM000673.2:g.67584726C>G GRCh38
NC_000011.9:g.67352197C>G , CM000673.1:g.67352197C>G GRCh37
NC_000011.8:g.67108773C>G NCBI36
NG_012075.1:g.6132C>G , LRG_723:g.6132C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.186C>G ENSP00000381604.1:p.Thr62=
ENST00000398606.10:c.186C>G MANE Select ENSP00000381607.3:p.Thr62=
ENST00000646888.1:c.79C>G ENSP00000494477.1:p.Pro27Ala
ENST00000398603.5:c.186C>G ENSP00000381604.1:p.Thr62=
ENST00000398606.7:c.186C>G ENSP00000381607.3:p.Thr62=
ENST00000489040.1:n.185C>G
ENST00000494593.1:n.616C>G
ENST00000498765.5:c.149C>G
NM_000852.3:c.186C>G , LRG_723t1:c.186C>G NP_000843.1:p.Thr62=
NM_000852.4:c.186C>G MANE Select NP_000843.1:p.Thr62=