Canonical Allele Identifier: CA585055321

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1367601653
• gnomAD v2: 8-128092238-C-A
• gnomAD v3: 8-127079993-C-A
• gnomAD v4: 8-127079993-C-A
• MyVariant Identifiers: chr8:g.128092238C>A (hg19) ; chr8:g.127079993C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079993C>A , CM000670.2:g.127079993C>A	GRCh38
NC_000008.10:g.128092238C>A , CM000670.1:g.128092238C>A	GRCh37
NC_000008.9:g.128161420C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.120C>A (PRNCR1)
NR_119373.1:n.102-860G>T (PCAT2)