Canonical Allele Identifier: CA1980213697
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1591099516
gnomAD v3: 11-67584593-G-C
gnomAD v4: 11-67584593-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584593G>C , CM000673.2:g.67584593G>C GRCh38
NC_000011.9:g.67352064G>C , CM000673.1:g.67352064G>C GRCh37
NC_000011.8:g.67108640G>C NCBI36
NG_012075.1:g.5999G>C , LRG_723:g.5999G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.144+23G>C ENSP00000381604.1:n.144+23G>C
ENST00000398606.10:c.144+23G>C MANE Select ENSP00000381607.3:n.144+23G>C
ENST00000646888.1:c.38-92G>C ENSP00000494477.1:n.38-92G>C
ENST00000398603.5:c.144+23G>C ENSP00000381604.1:n.144+23G>C
ENST00000398606.7:c.144+23G>C ENSP00000381607.3:n.144+23G>C
ENST00000489040.1:n.143+23G>C
ENST00000494593.1:n.483G>C
ENST00000498765.5:c.107+23G>C
NM_000852.3:c.144+23G>C , LRG_723t1:c.144+23G>C NP_000843.1:n.144+23G>C
NM_000852.4:c.144+23G>C MANE Select NP_000843.1:n.144+23G>C
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