Canonical Allele Identifier: CA185700255

Gene: PRNCR1

Linked Data

• dbSNP Id: rs34446482
• MyVariant Identifiers: chr8:g.128104064_128104065insG (hg19) ; chr8:g.127091819_127091820insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091821dup , CM000670.2:g.127091821dup	GRCh38
NC_000008.10:g.128104066dup , CM000670.1:g.128104066dup	GRCh37
NC_000008.9:g.128173248dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11948dup