Canonical Allele Identifier: CA600237030
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1200064413
gnomAD v2: 11-67353286-T-C
gnomAD v3: 11-67585815-T-C
gnomAD v4: 11-67585815-T-C
MyVariant Identifiers: chr11:g.67353286T>C (hg19) chr11:g.67585815T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585815T>C , CM000673.2:g.67585815T>C GRCh38
NC_000011.9:g.67353286T>C , CM000673.1:g.67353286T>C GRCh37
NC_000011.8:g.67109862T>C NCBI36
NG_012075.1:g.7221T>C , LRG_723:g.7221T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-574T>C ENSP00000381604.1:n.337-574T>C
ENST00000398606.10:c.337-289T>C MANE Select ENSP00000381607.3:n.337-289T>C
ENST00000646888.1:c.*53-289T>C ENSP00000494477.1:n.*53-289T>C
ENST00000398603.5:c.337-574T>C ENSP00000381604.1:n.337-574T>C
ENST00000398606.7:c.337-289T>C ENSP00000381607.3:n.337-289T>C
ENST00000467591.1:n.448-289T>C
ENST00000494593.1:n.1132-289T>C
ENST00000498765.5:c.400-289T>C
NM_000852.3:c.337-289T>C , LRG_723t1:c.337-289T>C NP_000843.1:n.337-289T>C
NM_000852.4:c.337-289T>C MANE Select NP_000843.1:n.337-289T>C
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