Canonical Allele Identifier: CA381523437
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67354028A>C (hg19) chr11:g.67586557A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586557A>C , CM000673.2:g.67586557A>C GRCh38
NC_000011.9:g.67354028A>C , CM000673.1:g.67354028A>C GRCh37
NC_000011.8:g.67110604A>C NCBI36
NG_012075.1:g.7963A>C , LRG_723:g.7963A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.505A>C ENSP00000381604.1:p.Asn169His
ENST00000398606.10:c.613A>C MANE Select ENSP00000381607.3:p.Asn205His
ENST00000398603.5:c.505A>C ENSP00000381604.1:p.Asn169His
ENST00000398606.7:c.613A>C ENSP00000381607.3:p.Asn205His
ENST00000467591.1:n.724A>C
ENST00000494593.1:n.1585A>C
ENST00000498765.5:c.676A>C
NM_000852.3:c.613A>C , LRG_723t1:c.613A>C NP_000843.1:p.Asn205His
NM_000852.4:c.613A>C MANE Select NP_000843.1:p.Asn205His
Search 100 bp 5'
Search 100 bp 3'