Canonical Allele Identifier: CA381517766
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352227C>A (hg19) chr11:g.67584756C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584756C>A , CM000673.2:g.67584756C>A GRCh38
NC_000011.9:g.67352227C>A , CM000673.1:g.67352227C>A GRCh37
NC_000011.8:g.67108803C>A NCBI36
NG_012075.1:g.6162C>A , LRG_723:g.6162C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.216C>A ENSP00000381604.1:p.His72Gln
ENST00000398606.10:c.216C>A MANE Select ENSP00000381607.3:p.His72Gln
ENST00000646888.1:c.109C>A ENSP00000494477.1:p.Pro37Thr
ENST00000398603.5:c.216C>A ENSP00000381604.1:p.His72Gln
ENST00000398606.7:c.216C>A ENSP00000381607.3:p.His72Gln
ENST00000489040.1:n.215C>A
ENST00000494593.1:n.646C>A
ENST00000498765.5:c.179C>A
NM_000852.3:c.216C>A , LRG_723t1:c.216C>A NP_000843.1:p.His72Gln
NM_000852.4:c.216C>A MANE Select NP_000843.1:p.His72Gln
Search 100 bp 5'
Search 100 bp 3'