Canonical Allele Identifier: CA2604535389

Gene: PRNCR1 PCAT2

Linked Data

• dbSNP Id: rs1813585028
• gnomAD v3: 8-127080248-T-G
• gnomAD v4: 8-127080248-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127080248T>G , CM000670.2:g.127080248T>G	GRCh38
NC_000008.10:g.128092493T>G , CM000670.1:g.128092493T>G	GRCh37
NC_000008.9:g.128161675T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109833.1:n.375T>G (PRNCR1)
NR_119373.1:n.102-1115A>C (PCAT2)