Canonical Allele Identifier: CA2628934217

Gene: PPIB

Linked Data

• gnomAD v4: 15-64162785-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162785C>T , CM000677.2:g.64162785C>T	GRCh38
NC_000015.9:g.64454984C>T , CM000677.1:g.64454984C>T	GRCh37
NC_000015.8:g.62242037C>T	NCBI36
NG_012979.1:g.5371G>A , LRG_10:g.5371G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+67G>A MANE Select	ENSP00000300026.4:n.135+67G>A
ENST00000561048.2:n.168+67G>A
ENST00000680158.1:c.135+67G>A	ENSP00000504873.1:n.135+67G>A
ENST00000681397.1:c.135+67G>A	ENSP00000506584.1:n.135+67G>A
ENST00000681658.1:c.30+172G>A	ENSP00000505431.1:n.30+172G>A
ENST00000300026.3:c.135+67G>A	ENSP00000300026.3:n.135+67G>A
ENST00000558492.1:n.155+67G>A
ENST00000561048.1:n.170+67G>A
NM_000942.4:c.135+67G>A , LRG_10t1:c.135+67G>A	NP_000933.1:n.135+67G>A
NM_000942.5:c.135+67G>A MANE Select	NP_000933.1:n.135+67G>A