Canonical Allele Identifier: CA185700202

Gene: PRNCR1

Linked Data

• dbSNP Id: rs542108961
• gnomAD v2: 8-128103737-G-A
• gnomAD v3: 8-127091492-G-A
• gnomAD v4: 8-127091492-G-A
• MyVariant Identifiers: chr8:g.128103737G>A (hg19) ; chr8:g.127091492G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091492G>A , CM000670.2:g.127091492G>A	GRCh38
NC_000008.10:g.128103737G>A , CM000670.1:g.128103737G>A	GRCh37
NC_000008.9:g.128172919G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11619G>A