Canonical Allele Identifier: CA490812792
Gene: PPIB HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.64452304T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160105T>C , CM000677.2:g.64160105T>C GRCh38
NC_000015.9:g.64452304T>C , CM000677.1:g.64452304T>C GRCh37
NC_000015.8:g.62239357T>C NCBI36
NG_012979.1:g.8051A>G , LRG_10:g.8051A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.342A>G MANE Select ENSP00000300026.4:p.Gly114=
ENST00000561048.2:n.375A>G
ENST00000680158.1:c.342A>G ENSP00000504873.1:p.Gly114=
ENST00000680343.1:n.296A>G
ENST00000681397.1:c.342A>G ENSP00000506584.1:p.Gly114=
ENST00000681658.1:c.237A>G ENSP00000505431.1:p.Gly79=
ENST00000300026.3:c.342A>G ENSP00000300026.3:p.Gly114=
ENST00000558492.1:n.248A>G
ENST00000561048.1:n.377A>G
NM_000942.4:c.342A>G , LRG_10t1:c.342A>G NP_000933.1:p.Gly114=
NM_000942.5:c.342A>G MANE Select NP_000933.1:p.Gly114=