Canonical Allele Identifier: CA322311206
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs994801526
gnomAD v3: 22-21658608-G-C
gnomAD v4: 22-21658608-G-C
MyVariant Identifiers: chr22:g.22012897G>C (hg19) chr22:g.21658608G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658608G>C , CM000684.2:g.21658608G>C GRCh38
NC_000022.10:g.22012897G>C , CM000684.1:g.22012897G>C GRCh37
NC_000022.9:g.20342897G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+219G>C
ENST00000498589.1:n.540-35G>C
XM_017029165.1:c.674+146G>C XP_016884654.1:n.674+146G>C
NR_169729.1:n.1420G>C
NR_169730.1:n.1323G>C
NR_169731.1:n.432-2229G>C
NR_169732.1:n.328+146G>C
NR_169733.1:n.387-35G>C
NR_169734.1:n.411-35G>C
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