Canonical Allele Identifier: CA381519104
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs990829761
MyVariant Identifiers: chr11:g.67352659G>C (hg19) chr11:g.67585188G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585188G>C , CM000673.2:g.67585188G>C GRCh38
NC_000011.9:g.67352659G>C , CM000673.1:g.67352659G>C GRCh37
NC_000011.8:g.67109235G>C NCBI36
NG_012075.1:g.6594G>C , LRG_723:g.6594G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.283G>C ENSP00000381604.1:p.Asp95His
ENST00000398606.10:c.283G>C MANE Select ENSP00000381607.3:p.Asp95His
ENST00000646888.1:c.176G>C ENSP00000494477.1:p.Ter59Ser
ENST00000398603.5:c.283G>C ENSP00000381604.1:p.Asp95His
ENST00000398606.7:c.283G>C ENSP00000381607.3:p.Asp95His
ENST00000467591.1:n.394G>C
ENST00000494593.1:n.1078G>C
ENST00000498765.5:c.346G>C
NM_000852.3:c.283G>C , LRG_723t1:c.283G>C NP_000843.1:p.Asp95His
NM_000852.4:c.283G>C MANE Select NP_000843.1:p.Asp95His
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