Canonical Allele Identifier: CA185700290

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1020401389
• gnomAD v3: 8-127092167-G-T
• gnomAD v4: 8-127092167-G-T
• MyVariant Identifiers: chr8:g.128104412G>T (hg19) ; chr8:g.127092167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092167G>T , CM000670.2:g.127092167G>T	GRCh38
NC_000008.10:g.128104412G>T , CM000670.1:g.128104412G>T	GRCh37
NC_000008.9:g.128173594G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12294G>T