Canonical Allele Identifier: CA490812795

Gene: PPIB

Linked Data

• ClinVar Variation Id: 3004564
• ClinVar RCV Id: RCV003860667
• dbSNP Id: rs2081557018
• gnomAD v3: 15-64160108-T-A
• gnomAD v4: 15-64160108-T-A
• MyVariant Identifiers: chr15:g.64452307T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160108T>A , CM000677.2:g.64160108T>A	GRCh38
NC_000015.9:g.64452307T>A , CM000677.1:g.64452307T>A	GRCh37
NC_000015.8:g.62239360T>A	NCBI36
NG_012979.1:g.8048A>T , LRG_10:g.8048A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.339A>T MANE Select	ENSP00000300026.4:p.Thr113=
ENST00000561048.2:n.372A>T
ENST00000680158.1:c.339A>T	ENSP00000504873.1:p.Thr113=
ENST00000680343.1:n.293A>T
ENST00000681397.1:c.339A>T	ENSP00000506584.1:p.Thr113=
ENST00000681658.1:c.234A>T	ENSP00000505431.1:p.Thr78=
ENST00000300026.3:c.339A>T	ENSP00000300026.3:p.Thr113=
ENST00000558492.1:n.245A>T
ENST00000561048.1:n.374A>T
NM_000942.4:c.339A>T , LRG_10t1:c.339A>T	NP_000933.1:p.Thr113=
NM_000942.5:c.339A>T MANE Select	NP_000933.1:p.Thr113=