Canonical Allele Identifier: CA185700235

Gene: PRNCR1

Linked Data

• dbSNP Id: rs773338080
• gnomAD v3: 8-127091717-T-G
• gnomAD v4: 8-127091717-T-G
• MyVariant Identifiers: chr8:g.128103962T>G (hg19) ; chr8:g.127091717T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091717T>G , CM000670.2:g.127091717T>G	GRCh38
NC_000008.10:g.128103962T>G , CM000670.1:g.128103962T>G	GRCh37
NC_000008.9:g.128173144T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11844T>G