Canonical Allele Identifier: CA2396906870
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs2066220534
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658472T>A , CM000684.2:g.21658472T>A GRCh38
NC_000022.10:g.22012761T>A , CM000684.1:g.22012761T>A GRCh37
NC_000022.9:g.20342761T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+83T>A
ENST00000498589.1:n.539+10T>A
XM_017029165.1:c.674+10T>A XP_016884654.1:n.674+10T>A
NR_169729.1:n.1284T>A
NR_169730.1:n.1187T>A
NR_169731.1:n.432-2365T>A
NR_169732.1:n.328+10T>A
NR_169733.1:n.386+10T>A
NR_169734.1:n.410+10T>A
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