Canonical Allele Identifier: CA6142748
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs752731774
ExAC: 11:67352223 G / A
gnomAD v2: 11-67352223-G-A
gnomAD v3: 11-67584752-G-A
gnomAD v4: 11-67584752-G-A
COSMIC: COSM4935079 COSM4935080
MyVariant Identifiers: chr11:g.67352223G>A (hg19) chr11:g.67584752G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584752G>A , CM000673.2:g.67584752G>A GRCh38
NC_000011.9:g.67352223G>A , CM000673.1:g.67352223G>A GRCh37
NC_000011.8:g.67108799G>A NCBI36
NG_012075.1:g.6158G>A , LRG_723:g.6158G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.212G>A ENSP00000381604.1:p.Arg71His
ENST00000398606.10:c.212G>A MANE Select ENSP00000381607.3:p.Arg71His
ENST00000646888.1:c.105G>A ENSP00000494477.1:p.Ala35=
ENST00000398603.5:c.212G>A ENSP00000381604.1:p.Arg71His
ENST00000398606.7:c.212G>A ENSP00000381607.3:p.Arg71His
ENST00000489040.1:n.211G>A
ENST00000494593.1:n.642G>A
ENST00000498765.5:c.175G>A
NM_000852.3:c.212G>A , LRG_723t1:c.212G>A NP_000843.1:p.Arg71His
NM_000852.4:c.212G>A MANE Select NP_000843.1:p.Arg71His
Search 100 bp 5'
Search 100 bp 3'