Canonical Allele Identifier: CA475394729
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352212T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584741T>C , CM000673.2:g.67584741T>C GRCh38
NC_000011.9:g.67352212T>C , CM000673.1:g.67352212T>C GRCh37
NC_000011.8:g.67108788T>C NCBI36
NG_012075.1:g.6147T>C , LRG_723:g.6147T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.201T>C ENSP00000381604.1:p.Asn67=
ENST00000398606.10:c.201T>C MANE Select ENSP00000381607.3:p.Asn67=
ENST00000646888.1:c.94T>C ENSP00000494477.1:p.Tyr32His
ENST00000398603.5:c.201T>C ENSP00000381604.1:p.Asn67=
ENST00000398606.7:c.201T>C ENSP00000381607.3:p.Asn67=
ENST00000489040.1:n.200T>C
ENST00000494593.1:n.631T>C
ENST00000498765.5:c.164T>C
NM_000852.3:c.201T>C , LRG_723t1:c.201T>C NP_000843.1:p.Asn67=
NM_000852.4:c.201T>C MANE Select NP_000843.1:p.Asn67=