Canonical Allele Identifier: CA7608637

Gene: PPIB

Linked Data

• ClinVar Variation Id: 1672923
• ClinVar RCV Id: RCV002210819
• dbSNP Id: rs148644836
• ExAC: 15:64455162 G / A
• gnomAD v2: 15-64455162-G-A
• gnomAD v3: 15-64162963-G-A
• gnomAD v4: 15-64162963-G-A
• MyVariant Identifiers: chr15:g.64455162G>A (hg19) ; chr15:g.64162963G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162963G>A , CM000677.2:g.64162963G>A	GRCh38
NC_000015.9:g.64455162G>A , CM000677.1:g.64455162G>A	GRCh37
NC_000015.8:g.62242215G>A	NCBI36
NG_012979.1:g.5193C>T , LRG_10:g.5193C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.24C>T MANE Select	ENSP00000300026.4:p.Asn8=
ENST00000561048.2:n.57C>T
ENST00000680158.1:c.24C>T	ENSP00000504873.1:p.Asn8=
ENST00000681397.1:c.24C>T	ENSP00000506584.1:p.Asn8=
ENST00000681658.1:c.24C>T	ENSP00000505431.1:p.Asn8=
ENST00000300026.3:c.24C>T	ENSP00000300026.3:p.Asn8=
ENST00000558492.1:n.44C>T
ENST00000561048.1:n.59C>T
NM_000942.4:c.24C>T , LRG_10t1:c.24C>T	NP_000933.1:p.Asn8=
NM_000942.5:c.24C>T MANE Select	NP_000933.1:p.Asn8=