Canonical Allele Identifier: CA381523227
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67354005C>A (hg19) chr11:g.67586534C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586534C>A , CM000673.2:g.67586534C>A GRCh38
NC_000011.9:g.67354005C>A , CM000673.1:g.67354005C>A GRCh37
NC_000011.8:g.67110581C>A NCBI36
NG_012075.1:g.7940C>A , LRG_723:g.7940C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.482C>A ENSP00000381604.1:p.Pro161His
ENST00000398606.10:c.590C>A MANE Select ENSP00000381607.3:p.Pro197His
ENST00000398603.5:c.482C>A ENSP00000381604.1:p.Pro161His
ENST00000398606.7:c.590C>A ENSP00000381607.3:p.Pro197His
ENST00000467591.1:n.701C>A
ENST00000494593.1:n.1562C>A
ENST00000498765.5:c.653C>A
NM_000852.3:c.590C>A , LRG_723t1:c.590C>A NP_000843.1:p.Pro197His
NM_000852.4:c.590C>A MANE Select NP_000843.1:p.Pro197His
Search 100 bp 5'
Search 100 bp 3'