Canonical Allele Identifier: CA475394542
Gene: GSTP1 HGNC NCBI

Linked Data

gnomAD v4: 11-67584693-G-C
MyVariant Identifiers: chr11:g.67352164G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584693G>C , CM000673.2:g.67584693G>C GRCh38
NC_000011.9:g.67352164G>C , CM000673.1:g.67352164G>C GRCh37
NC_000011.8:g.67108740G>C NCBI36
NG_012075.1:g.6099G>C , LRG_723:g.6099G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.153G>C ENSP00000381604.1:p.Gly51=
ENST00000398606.10:c.153G>C MANE Select ENSP00000381607.3:p.Gly51=
ENST00000646888.1:c.46G>C ENSP00000494477.1:p.Ala16Pro
ENST00000398603.5:c.153G>C ENSP00000381604.1:p.Gly51=
ENST00000398606.7:c.153G>C ENSP00000381607.3:p.Gly51=
ENST00000489040.1:n.152G>C
ENST00000494593.1:n.583G>C
ENST00000498765.5:c.116G>C
NM_000852.3:c.153G>C , LRG_723t1:c.153G>C NP_000843.1:p.Gly51=
NM_000852.4:c.153G>C MANE Select NP_000843.1:p.Gly51=
Search 100 bp 5'
Search 100 bp 3'