Canonical Allele Identifier: CA185698801

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs77236771
• gnomAD v2: 8-128092501-G-A
• gnomAD v3: 8-127080256-G-A
• gnomAD v4: 8-127080256-G-A
• MyVariant Identifiers: chr8:g.128092501G>A (hg19) ; chr8:g.127080256G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080256G>A , CM000670.2:g.127080256G>A	GRCh38
NC_000008.10:g.128092501G>A , CM000670.1:g.128092501G>A	GRCh37
NC_000008.9:g.128161683G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.383G>A (PRNCR1)
NR_119373.1:n.102-1123C>T (PCAT2)