Canonical Allele Identifier: CA585058090

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1419301836
• gnomAD v2: 8-128103903-G-A
• gnomAD v3: 8-127091658-G-A
• gnomAD v4: 8-127091658-G-A
• MyVariant Identifiers: chr8:g.128103903G>A (hg19) ; chr8:g.127091658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091658G>A , CM000670.2:g.127091658G>A	GRCh38
NC_000008.10:g.128103903G>A , CM000670.1:g.128103903G>A	GRCh37
NC_000008.9:g.128173085G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.11785G>A