Canonical Allele Identifier: CA2628934207
Gene: PPIB HGNC NCBI

Linked Data

gnomAD v4: 15-64162774-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162774G>C , CM000677.2:g.64162774G>C GRCh38
NC_000015.9:g.64454973G>C , CM000677.1:g.64454973G>C GRCh37
NC_000015.8:g.62242026G>C NCBI36
NG_012979.1:g.5382C>G , LRG_10:g.5382C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+78C>G MANE Select ENSP00000300026.4:n.135+78C>G
ENST00000561048.2:n.168+78C>G
ENST00000680158.1:c.135+78C>G ENSP00000504873.1:n.135+78C>G
ENST00000681397.1:c.135+78C>G ENSP00000506584.1:n.135+78C>G
ENST00000681658.1:c.30+183C>G ENSP00000505431.1:n.30+183C>G
ENST00000300026.3:c.135+78C>G ENSP00000300026.3:n.135+78C>G
ENST00000558492.1:n.155+78C>G
ENST00000561048.1:n.170+78C>G
NM_000942.4:c.135+78C>G , LRG_10t1:c.135+78C>G NP_000933.1:n.135+78C>G
NM_000942.5:c.135+78C>G MANE Select NP_000933.1:n.135+78C>G
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