Canonical Allele Identifier: CA185700199

Gene: PRNCR1

Linked Data

• dbSNP Id: rs572758784
• gnomAD v2: 8-128103716-A-G
• gnomAD v3: 8-127091471-A-G
• gnomAD v4: 8-127091471-A-G
• MyVariant Identifiers: chr8:g.128103716A>G (hg19) ; chr8:g.127091471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091471A>G , CM000670.2:g.127091471A>G	GRCh38
NC_000008.10:g.128103716A>G , CM000670.1:g.128103716A>G	GRCh37
NC_000008.9:g.128172898A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11598A>G