Canonical Allele Identifier: CA490814681

Gene: PPIB

Linked Data

• dbSNP Id: rs1301621606
• gnomAD v2: 15-64455117-G-A
• gnomAD v3: 15-64162918-G-A
• gnomAD v4: 15-64162918-G-A
• MyVariant Identifiers: chr15:g.64455117G>A (hg19) ; chr15:g.64162918G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162918G>A , CM000677.2:g.64162918G>A	GRCh38
NC_000015.9:g.64455117G>A , CM000677.1:g.64455117G>A	GRCh37
NC_000015.8:g.62242170G>A	NCBI36
NG_012979.1:g.5238C>T , LRG_10:g.5238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.69C>T MANE Select	ENSP00000300026.4:p.Phe23=
ENST00000561048.2:n.102C>T
ENST00000680158.1:c.69C>T	ENSP00000504873.1:p.Phe23=
ENST00000681397.1:c.69C>T	ENSP00000506584.1:p.Phe23=
ENST00000681658.1:c.30+39C>T	ENSP00000505431.1:n.30+39C>T
ENST00000300026.3:c.69C>T	ENSP00000300026.3:p.Phe23=
ENST00000558492.1:n.89C>T
ENST00000561048.1:n.104C>T
NM_000942.4:c.69C>T , LRG_10t1:c.69C>T	NP_000933.1:p.Phe23=
NM_000942.5:c.69C>T MANE Select	NP_000933.1:p.Phe23=