Canonical Allele Identifier: CA513535509
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012695C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658406C>G , CM000684.2:g.21658406C>G GRCh38
NC_000022.10:g.22012695C>G , CM000684.1:g.22012695C>G GRCh37
NC_000022.9:g.20342695C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+17C>G
ENST00000498589.1:n.483C>G
XM_017029165.1:c.618C>G XP_016884654.1:p.Leu206=
NR_169729.1:n.1218C>G
NR_169730.1:n.1121C>G
NR_169731.1:n.432-2431C>G
NR_169732.1:n.272C>G
NR_169733.1:n.330C>G
NR_169734.1:n.354C>G