Canonical Allele Identifier: CA513535277

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012622A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658333A>T , CM000684.2:g.21658333A>T	GRCh38
NC_000022.10:g.22012622A>T , CM000684.1:g.22012622A>T	GRCh37
NC_000022.9:g.20342622A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.230A>T
ENST00000498589.1:n.410A>T
XM_017029165.1:c.545A>T	XP_016884654.1:p.His182Leu
NR_169729.1:n.1145A>T
NR_169730.1:n.1048A>T
NR_169731.1:n.432-2504A>T
NR_169732.1:n.199A>T
NR_169733.1:n.257A>T
NR_169734.1:n.281A>T