Canonical Allele Identifier: CA513535276

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012621C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658332C>G , CM000684.2:g.21658332C>G	GRCh38
NC_000022.10:g.22012621C>G , CM000684.1:g.22012621C>G	GRCh37
NC_000022.9:g.20342621C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.229C>G
ENST00000498589.1:n.409C>G
XM_017029165.1:c.544C>G	XP_016884654.1:p.His182Asp
NR_169729.1:n.1144C>G
NR_169730.1:n.1047C>G
NR_169731.1:n.432-2505C>G
NR_169732.1:n.198C>G
NR_169733.1:n.256C>G
NR_169734.1:n.280C>G