Canonical Allele Identifier: CA2628934203

Gene: PPIB

Linked Data

• gnomAD v4: 15-64162771-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162771G>A , CM000677.2:g.64162771G>A	GRCh38
NC_000015.9:g.64454970G>A , CM000677.1:g.64454970G>A	GRCh37
NC_000015.8:g.62242023G>A	NCBI36
NG_012979.1:g.5385C>T , LRG_10:g.5385C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+81C>T MANE Select	ENSP00000300026.4:n.135+81C>T
ENST00000561048.2:n.168+81C>T
ENST00000680158.1:c.135+81C>T	ENSP00000504873.1:n.135+81C>T
ENST00000681397.1:c.135+81C>T	ENSP00000506584.1:n.135+81C>T
ENST00000681658.1:c.30+186C>T	ENSP00000505431.1:n.30+186C>T
ENST00000300026.3:c.135+81C>T	ENSP00000300026.3:n.135+81C>T
ENST00000558492.1:n.155+81C>T
ENST00000561048.1:n.170+81C>T
NM_000942.4:c.135+81C>T , LRG_10t1:c.135+81C>T	NP_000933.1:n.135+81C>T
NM_000942.5:c.135+81C>T MANE Select	NP_000933.1:n.135+81C>T