Canonical Allele Identifier: CA1980214302
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1867441145

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584949G>A , CM000673.2:g.67584949G>A GRCh38
NC_000011.9:g.67352420G>A , CM000673.1:g.67352420G>A GRCh37
NC_000011.8:g.67108996G>A NCBI36
NG_012075.1:g.6355G>A , LRG_723:g.6355G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.232+177G>A ENSP00000381604.1:n.232+177G>A
ENST00000398606.10:c.232+177G>A MANE Select ENSP00000381607.3:n.232+177G>A
ENST00000646888.1:c.125+177G>A ENSP00000494477.1:n.125+177G>A
ENST00000398603.5:c.232+177G>A ENSP00000381604.1:n.232+177G>A
ENST00000398606.7:c.232+177G>A ENSP00000381607.3:n.232+177G>A
ENST00000467591.1:n.155G>A
ENST00000489040.1:n.408G>A
ENST00000494593.1:n.839G>A
ENST00000498765.5:c.196-89G>A
NM_000852.3:c.232+177G>A , LRG_723t1:c.232+177G>A NP_000843.1:n.232+177G>A
NM_000852.4:c.232+177G>A MANE Select NP_000843.1:n.232+177G>A