Canonical Allele Identifier: CA2628934204

Gene: PPIB

Linked Data

• gnomAD v4: 15-64162772-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162772A>G , CM000677.2:g.64162772A>G	GRCh38
NC_000015.9:g.64454971A>G , CM000677.1:g.64454971A>G	GRCh37
NC_000015.8:g.62242024A>G	NCBI36
NG_012979.1:g.5384T>C , LRG_10:g.5384T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+80T>C MANE Select	ENSP00000300026.4:n.135+80T>C
ENST00000561048.2:n.168+80T>C
ENST00000680158.1:c.135+80T>C	ENSP00000504873.1:n.135+80T>C
ENST00000681397.1:c.135+80T>C	ENSP00000506584.1:n.135+80T>C
ENST00000681658.1:c.30+185T>C	ENSP00000505431.1:n.30+185T>C
ENST00000300026.3:c.135+80T>C	ENSP00000300026.3:n.135+80T>C
ENST00000558492.1:n.155+80T>C
ENST00000561048.1:n.170+80T>C
NM_000942.4:c.135+80T>C , LRG_10t1:c.135+80T>C	NP_000933.1:n.135+80T>C
NM_000942.5:c.135+80T>C MANE Select	NP_000933.1:n.135+80T>C