Canonical Allele Identifier: CA2655514826
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658485-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658485T>C , CM000684.2:g.21658485T>C GRCh38
NC_000022.10:g.22012774T>C , CM000684.1:g.22012774T>C GRCh37
NC_000022.9:g.20342774T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+96T>C
ENST00000498589.1:n.539+23T>C
XM_017029165.1:c.674+23T>C XP_016884654.1:n.674+23T>C
NR_169729.1:n.1297T>C
NR_169730.1:n.1200T>C
NR_169731.1:n.432-2352T>C
NR_169732.1:n.328+23T>C
NR_169733.1:n.386+23T>C
NR_169734.1:n.410+23T>C
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