Canonical Allele Identifier: CA585058076

Gene: PRNCR1

Linked Data

• dbSNP Id: rs770997417
• gnomAD v2: 8-128103847-C-G
• gnomAD v3: 8-127091602-C-G
• gnomAD v4: 8-127091602-C-G
• MyVariant Identifiers: chr8:g.128103847C>G (hg19) ; chr8:g.127091602C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091602C>G , CM000670.2:g.127091602C>G	GRCh38
NC_000008.10:g.128103847C>G , CM000670.1:g.128103847C>G	GRCh37
NC_000008.9:g.128173029C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.11729C>G