Canonical Allele Identifier: CA381515749
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352186G>C (hg19) chr11:g.67584715G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584715G>C , CM000673.2:g.67584715G>C GRCh38
NC_000011.9:g.67352186G>C , CM000673.1:g.67352186G>C GRCh37
NC_000011.8:g.67108762G>C NCBI36
NG_012075.1:g.6121G>C , LRG_723:g.6121G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.175G>C ENSP00000381604.1:p.Gly59Arg
ENST00000398606.10:c.175G>C MANE Select ENSP00000381607.3:p.Gly59Arg
ENST00000646888.1:c.68G>C ENSP00000494477.1:p.Arg23Pro
ENST00000398603.5:c.175G>C ENSP00000381604.1:p.Gly59Arg
ENST00000398606.7:c.175G>C ENSP00000381607.3:p.Gly59Arg
ENST00000489040.1:n.174G>C
ENST00000494593.1:n.605G>C
ENST00000498765.5:c.138G>C
NM_000852.3:c.175G>C , LRG_723t1:c.175G>C NP_000843.1:p.Gly59Arg
NM_000852.4:c.175G>C MANE Select NP_000843.1:p.Gly59Arg
Search 100 bp 5'
Search 100 bp 3'