Canonical Allele Identifier: CA585058146

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1383346866
• gnomAD v2: 8-128104386-T-C
• gnomAD v3: 8-127092141-T-C
• gnomAD v4: 8-127092141-T-C
• MyVariant Identifiers: chr8:g.128104386T>C (hg19) ; chr8:g.127092141T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092141T>C , CM000670.2:g.127092141T>C	GRCh38
NC_000008.10:g.128104386T>C , CM000670.1:g.128104386T>C	GRCh37
NC_000008.9:g.128173568T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12268T>C