Canonical Allele Identifier: CA513535207

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012598A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658309A>C , CM000684.2:g.21658309A>C	GRCh38
NC_000022.10:g.22012598A>C , CM000684.1:g.22012598A>C	GRCh37
NC_000022.9:g.20342598A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.206A>C
ENST00000498589.1:n.386A>C
XM_017029165.1:c.521A>C	XP_016884654.1:p.Asn174Thr
NR_169729.1:n.1121A>C
NR_169730.1:n.1024A>C
NR_169731.1:n.432-2528A>C
NR_169732.1:n.175A>C
NR_169733.1:n.233A>C
NR_169734.1:n.257A>C