Canonical Allele Identifier: CA6142918
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs376074280
ExAC: 11:67354017 A / C
gnomAD v2: 11-67354017-A-C
gnomAD v3: 11-67586546-A-C
gnomAD v4: 11-67586546-A-C
MyVariant Identifiers: chr11:g.67354017A>C (hg19) chr11:g.67586546A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586546A>C , CM000673.2:g.67586546A>C GRCh38
NC_000011.9:g.67354017A>C , CM000673.1:g.67354017A>C GRCh37
NC_000011.8:g.67110593A>C NCBI36
NG_012075.1:g.7952A>C , LRG_723:g.7952A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.494A>C ENSP00000381604.1:p.Asn165Thr
ENST00000398606.10:c.602A>C MANE Select ENSP00000381607.3:p.Asn201Thr
ENST00000398603.5:c.494A>C ENSP00000381604.1:p.Asn165Thr
ENST00000398606.7:c.602A>C ENSP00000381607.3:p.Asn201Thr
ENST00000467591.1:n.713A>C
ENST00000494593.1:n.1574A>C
ENST00000498765.5:c.665A>C
NM_000852.3:c.602A>C , LRG_723t1:c.602A>C NP_000843.1:p.Asn201Thr
NM_000852.4:c.602A>C MANE Select NP_000843.1:p.Asn201Thr
Search 100 bp 5'
Search 100 bp 3'