Canonical Allele Identifier: CA847146839

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1421735027
• MyVariant Identifiers: chr8:g.128104184_128104185insC (hg19) ; chr8:g.127091939_127091940insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091942dup , CM000670.2:g.127091942dup	GRCh38
NC_000008.10:g.128104187dup , CM000670.1:g.128104187dup	GRCh37
NC_000008.9:g.128173369dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12069dup