Canonical Allele Identifier: CA185700239

Gene: PRNCR1

Linked Data

• dbSNP Id: rs5013678
• gnomAD v2: 8-128103979-T-C
• gnomAD v3: 8-127091734-T-C
• gnomAD v4: 8-127091734-T-C
• MyVariant Identifiers: chr8:g.128103979T>C (hg19) ; chr8:g.127091734T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091734T>C , CM000670.2:g.127091734T>C	GRCh38
NC_000008.10:g.128103979T>C , CM000670.1:g.128103979T>C	GRCh37
NC_000008.9:g.128173161T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11861T>C