Canonical Allele Identifier: CA185700201

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1052880812
• gnomAD v2: 8-128103736-C-T
• gnomAD v3: 8-127091491-C-T
• gnomAD v4: 8-127091491-C-T
• MyVariant Identifiers: chr8:g.128103736C>T (hg19) ; chr8:g.127091491C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091491C>T , CM000670.2:g.127091491C>T	GRCh38
NC_000008.10:g.128103736C>T , CM000670.1:g.128103736C>T	GRCh37
NC_000008.9:g.128172918C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11618C>T