Canonical Allele Identifier: CA475394630
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352188A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584717A>C , CM000673.2:g.67584717A>C GRCh38
NC_000011.9:g.67352188A>C , CM000673.1:g.67352188A>C GRCh37
NC_000011.8:g.67108764A>C NCBI36
NG_012075.1:g.6123A>C , LRG_723:g.6123A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.177A>C ENSP00000381604.1:p.Gly59=
ENST00000398606.10:c.177A>C MANE Select ENSP00000381607.3:p.Gly59=
ENST00000646888.1:c.70A>C ENSP00000494477.1:p.Arg24=
ENST00000398603.5:c.177A>C ENSP00000381604.1:p.Gly59=
ENST00000398606.7:c.177A>C ENSP00000381607.3:p.Gly59=
ENST00000489040.1:n.176A>C
ENST00000494593.1:n.607A>C
ENST00000498765.5:c.140A>C
NM_000852.3:c.177A>C , LRG_723t1:c.177A>C NP_000843.1:p.Gly59=
NM_000852.4:c.177A>C MANE Select NP_000843.1:p.Gly59=