Canonical Allele Identifier: CA679523413
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1280123792
MyVariant Identifiers: chr11:g.67353771G>A (hg19) chr11:g.67586300G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586300G>A , CM000673.2:g.67586300G>A GRCh38
NC_000011.9:g.67353771G>A , CM000673.1:g.67353771G>A GRCh37
NC_000011.8:g.67110347G>A NCBI36
NG_012075.1:g.7706G>A , LRG_723:g.7706G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-89G>A ENSP00000381604.1:n.337-89G>A
ENST00000398606.10:c.445-89G>A MANE Select ENSP00000381607.3:n.445-89G>A
ENST00000646888.1:c.*161-89G>A ENSP00000494477.1:n.*161-89G>A
ENST00000398603.5:c.337-89G>A ENSP00000381604.1:n.337-89G>A
ENST00000398606.7:c.445-89G>A ENSP00000381607.3:n.445-89G>A
ENST00000467591.1:n.556-89G>A
ENST00000494593.1:n.1328G>A
ENST00000495996.1:c.170+27G>A ENSP00000484686.1:n.170+27G>A
ENST00000498765.5:c.508-89G>A
NM_000852.3:c.445-89G>A , LRG_723t1:c.445-89G>A NP_000843.1:n.445-89G>A
NM_000852.4:c.445-89G>A MANE Select NP_000843.1:n.445-89G>A
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