Canonical Allele Identifier: CA1118986279

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813584610
• gnomAD v3: 8-127080225-A-T
• gnomAD v4: 8-127080225-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080225A>T , CM000670.2:g.127080225A>T	GRCh38
NC_000008.10:g.128092470A>T , CM000670.1:g.128092470A>T	GRCh37
NC_000008.9:g.128161652A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.352A>T (PRNCR1)
NR_119373.1:n.102-1092T>A (PCAT2)