Canonical Allele Identifier: CA475395140
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352236C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584765C>A , CM000673.2:g.67584765C>A GRCh38
NC_000011.9:g.67352236C>A , CM000673.1:g.67352236C>A GRCh37
NC_000011.8:g.67108812C>A NCBI36
NG_012075.1:g.6171C>A , LRG_723:g.6171C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.225C>A ENSP00000381604.1:p.Arg75=
ENST00000398606.10:c.225C>A MANE Select ENSP00000381607.3:p.Arg75=
ENST00000646888.1:c.118C>A ENSP00000494477.1:p.His40Asn
ENST00000398603.5:c.225C>A ENSP00000381604.1:p.Arg75=
ENST00000398606.7:c.225C>A ENSP00000381607.3:p.Arg75=
ENST00000489040.1:n.224C>A
ENST00000494593.1:n.655C>A
ENST00000498765.5:c.188C>A
NM_000852.3:c.225C>A , LRG_723t1:c.225C>A NP_000843.1:p.Arg75=
NM_000852.4:c.225C>A MANE Select NP_000843.1:p.Arg75=