Canonical Allele Identifier: CA679520359
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs981849351
gnomAD v3: 11-67583611-G-A
gnomAD v4: 11-67583611-G-A
MyVariant Identifiers: chr11:g.67351082G>A (hg19) chr11:g.67583611G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67583611G>A , CM000673.2:g.67583611G>A GRCh38
NC_000011.9:g.67351082G>A , CM000673.1:g.67351082G>A GRCh37
NC_000011.8:g.67107658G>A NCBI36
NG_012075.1:g.5017G>A , LRG_723:g.5017G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398606.7:c.-233G>A ENSP00000381607.3:n.-233G>A
NM_000852.3:c.-233G>A , LRG_723t1:c.-233G>A NP_000843.1:n.-233G>A
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