Canonical Allele Identifier: CA475394744
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352215C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584744C>A , CM000673.2:g.67584744C>A GRCh38
NC_000011.9:g.67352215C>A , CM000673.1:g.67352215C>A GRCh37
NC_000011.8:g.67108791C>A NCBI36
NG_012075.1:g.6150C>A , LRG_723:g.6150C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.204C>A ENSP00000381604.1:p.Thr68=
ENST00000398606.10:c.204C>A MANE Select ENSP00000381607.3:p.Thr68=
ENST00000646888.1:c.97C>A ENSP00000494477.1:p.His33Asn
ENST00000398603.5:c.204C>A ENSP00000381604.1:p.Thr68=
ENST00000398606.7:c.204C>A ENSP00000381607.3:p.Thr68=
ENST00000489040.1:n.203C>A
ENST00000494593.1:n.634C>A
ENST00000498765.5:c.167C>A
NM_000852.3:c.204C>A , LRG_723t1:c.204C>A NP_000843.1:p.Thr68=
NM_000852.4:c.204C>A MANE Select NP_000843.1:p.Thr68=