Canonical Allele Identifier: CA475395969
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134395224
MyVariant Identifiers: chr11:g.67353598G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586127G>A , CM000673.2:g.67586127G>A GRCh38
NC_000011.9:g.67353598G>A , CM000673.1:g.67353598G>A GRCh37
NC_000011.8:g.67110174G>A NCBI36
NG_012075.1:g.7533G>A , LRG_723:g.7533G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-262G>A ENSP00000381604.1:n.337-262G>A
ENST00000398606.10:c.360G>A MANE Select ENSP00000381607.3:p.Val120=
ENST00000646888.1:c.*76G>A ENSP00000494477.1:n.*76G>A
ENST00000398603.5:c.337-262G>A ENSP00000381604.1:n.337-262G>A
ENST00000398606.7:c.360G>A ENSP00000381607.3:p.Val120=
ENST00000467591.1:n.471G>A
ENST00000494593.1:n.1155G>A
ENST00000495996.1:c.24G>A ENSP00000484686.1:p.Val8=
ENST00000498765.5:c.423G>A
NM_000852.3:c.360G>A , LRG_723t1:c.360G>A NP_000843.1:p.Val120=
NM_000852.4:c.360G>A MANE Select NP_000843.1:p.Val120=