Canonical Allele Identifier: CA392819805
Gene: PPIB HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.64455077T>C (hg19) chr15:g.64162878T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162878T>C , CM000677.2:g.64162878T>C GRCh38
NC_000015.9:g.64455077T>C , CM000677.1:g.64455077T>C GRCh37
NC_000015.8:g.62242130T>C NCBI36
NG_012979.1:g.5278A>G , LRG_10:g.5278A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.109A>G MANE Select ENSP00000300026.4:p.Lys37Glu
ENST00000561048.2:n.142A>G
ENST00000680158.1:c.109A>G ENSP00000504873.1:p.Lys37Glu
ENST00000681397.1:c.109A>G ENSP00000506584.1:p.Lys37Glu
ENST00000681658.1:c.30+79A>G ENSP00000505431.1:n.30+79A>G
ENST00000300026.3:c.109A>G ENSP00000300026.3:p.Lys37Glu
ENST00000558492.1:n.129A>G
ENST00000561048.1:n.144A>G
NM_000942.4:c.109A>G , LRG_10t1:c.109A>G NP_000933.1:p.Lys37Glu
NM_000942.5:c.109A>G MANE Select NP_000933.1:p.Lys37Glu
Search 100 bp 5'
Search 100 bp 3'