Canonical Allele Identifier: CA185700241

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1039830248
• gnomAD v3: 8-127091741-A-G
• gnomAD v4: 8-127091741-A-G
• MyVariant Identifiers: chr8:g.128103986A>G (hg19) ; chr8:g.127091741A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091741A>G , CM000670.2:g.127091741A>G	GRCh38
NC_000008.10:g.128103986A>G , CM000670.1:g.128103986A>G	GRCh37
NC_000008.9:g.128173168A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.11868A>G