Canonical Allele Identifier: CA585058148

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1294761551
• gnomAD v2: 8-128104397-C-CA
• gnomAD v4: 8-127092152-C-CA
• MyVariant Identifiers: chr8:g.128104397_128104398insA (hg19) ; chr8:g.127092152_127092153insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092158dup , CM000670.2:g.127092158dup	GRCh38
NC_000008.10:g.128104403dup , CM000670.1:g.128104403dup	GRCh37
NC_000008.9:g.128173585dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12285dup