Canonical Allele Identifier: CA392819949
Gene: PPIB HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.64455151A>C (hg19) chr15:g.64162952A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162952A>C , CM000677.2:g.64162952A>C GRCh38
NC_000015.9:g.64455151A>C , CM000677.1:g.64455151A>C GRCh37
NC_000015.8:g.62242204A>C NCBI36
NG_012979.1:g.5204T>G , LRG_10:g.5204T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.35T>G MANE Select ENSP00000300026.4:p.Leu12Arg
ENST00000561048.2:n.68T>G
ENST00000680158.1:c.35T>G ENSP00000504873.1:p.Leu12Arg
ENST00000681397.1:c.35T>G ENSP00000506584.1:p.Leu12Arg
ENST00000681658.1:c.30+5T>G ENSP00000505431.1:n.30+5T>G
ENST00000300026.3:c.35T>G ENSP00000300026.3:p.Leu12Arg
ENST00000558492.1:n.55T>G
ENST00000561048.1:n.70T>G
NM_000942.4:c.35T>G , LRG_10t1:c.35T>G NP_000933.1:p.Leu12Arg
NM_000942.5:c.35T>G MANE Select NP_000933.1:p.Leu12Arg
Search 100 bp 5'
Search 100 bp 3'