Canonical Allele Identifier: CA475395295
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1451964684
MyVariant Identifiers: chr11:g.67352685A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585214A>G , CM000673.2:g.67585214A>G GRCh38
NC_000011.9:g.67352685A>G , CM000673.1:g.67352685A>G GRCh37
NC_000011.8:g.67109261A>G NCBI36
NG_012075.1:g.6620A>G , LRG_723:g.6620A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.309A>G ENSP00000381604.1:p.Lys103=
ENST00000398606.10:c.309A>G MANE Select ENSP00000381607.3:p.Lys103=
ENST00000646888.1:c.*25A>G ENSP00000494477.1:n.*25A>G
ENST00000398603.5:c.309A>G ENSP00000381604.1:p.Lys103=
ENST00000398606.7:c.309A>G ENSP00000381607.3:p.Lys103=
ENST00000467591.1:n.420A>G
ENST00000494593.1:n.1104A>G
ENST00000498765.5:c.372A>G
NM_000852.3:c.309A>G , LRG_723t1:c.309A>G NP_000843.1:p.Lys103=
NM_000852.4:c.309A>G MANE Select NP_000843.1:p.Lys103=