Canonical Allele Identifier: CA7608629
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs746610540

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162942G>A , CM000677.2:g.64162942G>A GRCh38
NC_000015.9:g.64455141G>A , CM000677.1:g.64455141G>A GRCh37
NC_000015.8:g.62242194G>A NCBI36
NG_012979.1:g.5214C>T , LRG_10:g.5214C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.45C>T MANE Select ENSP00000300026.4:p.Ala15=
ENST00000561048.2:n.78C>T
ENST00000680158.1:c.45C>T ENSP00000504873.1:p.Ala15=
ENST00000681397.1:c.45C>T ENSP00000506584.1:p.Ala15=
ENST00000681658.1:c.30+15C>T ENSP00000505431.1:n.30+15C>T
ENST00000300026.3:c.45C>T ENSP00000300026.3:p.Ala15=
ENST00000558492.1:n.65C>T
ENST00000561048.1:n.80C>T
NM_000942.4:c.45C>T , LRG_10t1:c.45C>T NP_000933.1:p.Ala15=
NM_000942.5:c.45C>T MANE Select NP_000933.1:p.Ala15=