Canonical Allele Identifier: CA679521648
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1452649341
MyVariant Identifiers: chr11:g.67352069G>A (hg19) chr11:g.67584598G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584598G>A , CM000673.2:g.67584598G>A GRCh38
NC_000011.9:g.67352069G>A , CM000673.1:g.67352069G>A GRCh37
NC_000011.8:g.67108645G>A NCBI36
NG_012075.1:g.6004G>A , LRG_723:g.6004G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.144+28G>A ENSP00000381604.1:n.144+28G>A
ENST00000398606.10:c.144+28G>A MANE Select ENSP00000381607.3:n.144+28G>A
ENST00000646888.1:c.38-87G>A ENSP00000494477.1:n.38-87G>A
ENST00000398603.5:c.144+28G>A ENSP00000381604.1:n.144+28G>A
ENST00000398606.7:c.144+28G>A ENSP00000381607.3:n.144+28G>A
ENST00000489040.1:n.143+28G>A
ENST00000494593.1:n.488G>A
ENST00000498765.5:c.107+28G>A
NM_000852.3:c.144+28G>A , LRG_723t1:c.144+28G>A NP_000843.1:n.144+28G>A
NM_000852.4:c.144+28G>A MANE Select NP_000843.1:n.144+28G>A
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