Canonical Allele Identifier: CA714834398

Gene: PPIB

Linked Data

• dbSNP Id: rs1169253566
• gnomAD v3: 15-64160004-A-T
• gnomAD v4: 15-64160004-A-T
• MyVariant Identifiers: chr15:g.64452203A>T (hg19) ; chr15:g.64160004A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160004A>T , CM000677.2:g.64160004A>T	GRCh38
NC_000015.9:g.64452203A>T , CM000677.1:g.64452203A>T	GRCh37
NC_000015.8:g.62239256A>T	NCBI36
NG_012979.1:g.8152T>A , LRG_10:g.8152T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.343+100T>A MANE Select	ENSP00000300026.4:n.343+100T>A
ENST00000561048.2:n.476T>A
ENST00000680158.1:c.343+100T>A	ENSP00000504873.1:n.343+100T>A
ENST00000680343.1:n.297+100T>A
ENST00000681397.1:c.343+100T>A	ENSP00000506584.1:n.343+100T>A
ENST00000681658.1:c.238+100T>A	ENSP00000505431.1:n.238+100T>A
ENST00000300026.3:c.343+100T>A	ENSP00000300026.3:n.343+100T>A
ENST00000558492.1:n.249+100T>A
ENST00000561048.1:n.478T>A
NM_000942.4:c.343+100T>A , LRG_10t1:c.343+100T>A	NP_000933.1:n.343+100T>A
NM_000942.5:c.343+100T>A MANE Select	NP_000933.1:n.343+100T>A