Canonical Allele Identifier: CA2655514841
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658490-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658490T>C , CM000684.2:g.21658490T>C GRCh38
NC_000022.10:g.22012779T>C , CM000684.1:g.22012779T>C GRCh37
NC_000022.9:g.20342779T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+101T>C
ENST00000498589.1:n.539+28T>C
XM_017029165.1:c.674+28T>C XP_016884654.1:n.674+28T>C
NR_169729.1:n.1302T>C
NR_169730.1:n.1205T>C
NR_169731.1:n.432-2347T>C
NR_169732.1:n.328+28T>C
NR_169733.1:n.386+28T>C
NR_169734.1:n.410+28T>C
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