Canonical Allele Identifier: CA224155077
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs879180925
gnomAD v4: 11-67586212-G-A
MyVariant Identifiers: chr11:g.67353683G>A (hg19) chr11:g.67586212G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586212G>A , CM000673.2:g.67586212G>A GRCh38
NC_000011.9:g.67353683G>A , CM000673.1:g.67353683G>A GRCh37
NC_000011.8:g.67110259G>A NCBI36
NG_012075.1:g.7618G>A , LRG_723:g.7618G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-177G>A ENSP00000381604.1:n.337-177G>A
ENST00000398606.10:c.444+1G>A MANE Select ENSP00000381607.3:n.444+1G>A
ENST00000646888.1:c.*160+1G>A ENSP00000494477.1:n.*160+1G>A
ENST00000398603.5:c.337-177G>A ENSP00000381604.1:n.337-177G>A
ENST00000398606.7:c.444+1G>A ENSP00000381607.3:n.444+1G>A
ENST00000467591.1:n.555+1G>A
ENST00000494593.1:n.1240G>A
ENST00000495996.1:c.109G>A ENSP00000484686.1:p.Val37Met
ENST00000498765.5:c.507+1G>A
NM_000852.3:c.444+1G>A , LRG_723t1:c.444+1G>A NP_000843.1:n.444+1G>A
NM_000852.4:c.444+1G>A MANE Select NP_000843.1:n.444+1G>A
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