Canonical Allele Identifier: CA475395321
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134394436
MyVariant Identifiers: chr11:g.67352706C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585235C>G , CM000673.2:g.67585235C>G GRCh38
NC_000011.9:g.67352706C>G , CM000673.1:g.67352706C>G GRCh37
NC_000011.8:g.67109282C>G NCBI36
NG_012075.1:g.6641C>G , LRG_723:g.6641C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.330C>G ENSP00000381604.1:p.Thr110=
ENST00000398606.10:c.330C>G MANE Select ENSP00000381607.3:p.Thr110=
ENST00000646888.1:c.*46C>G ENSP00000494477.1:n.*46C>G
ENST00000398603.5:c.330C>G ENSP00000381604.1:p.Thr110=
ENST00000398606.7:c.330C>G ENSP00000381607.3:p.Thr110=
ENST00000467591.1:n.441C>G
ENST00000494593.1:n.1125C>G
ENST00000498765.5:c.393C>G
NM_000852.3:c.330C>G , LRG_723t1:c.330C>G NP_000843.1:p.Thr110=
NM_000852.4:c.330C>G MANE Select NP_000843.1:p.Thr110=