Canonical Allele Identifier: CA475396024
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1867463473
MyVariant Identifiers: chr11:g.67353616A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586145A>G , CM000673.2:g.67586145A>G GRCh38
NC_000011.9:g.67353616A>G , CM000673.1:g.67353616A>G GRCh37
NC_000011.8:g.67110192A>G NCBI36
NG_012075.1:g.7551A>G , LRG_723:g.7551A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-244A>G ENSP00000381604.1:n.337-244A>G
ENST00000398606.10:c.378A>G MANE Select ENSP00000381607.3:p.Gln126=
ENST00000646888.1:c.*94A>G ENSP00000494477.1:n.*94A>G
ENST00000398603.5:c.337-244A>G ENSP00000381604.1:n.337-244A>G
ENST00000398606.7:c.378A>G ENSP00000381607.3:p.Gln126=
ENST00000467591.1:n.489A>G
ENST00000494593.1:n.1173A>G
ENST00000495996.1:c.42A>G ENSP00000484686.1:p.Gln14=
ENST00000498765.5:c.441A>G
NM_000852.3:c.378A>G , LRG_723t1:c.378A>G NP_000843.1:p.Gln126=
NM_000852.4:c.378A>G MANE Select NP_000843.1:p.Gln126=