Canonical Allele Identifier: CA847146810

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1228791004
• gnomAD v3: 8-127091913-T-C
• gnomAD v4: 8-127091913-T-C
• MyVariant Identifiers: chr8:g.128104158T>C (hg19) ; chr8:g.127091913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091913T>C , CM000670.2:g.127091913T>C	GRCh38
NC_000008.10:g.128104158T>C , CM000670.1:g.128104158T>C	GRCh37
NC_000008.9:g.128173340T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12040T>C