Canonical Allele Identifier: CA1118986171
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813579639
gnomAD v3: 8-127079920-A-G
gnomAD v4: 8-127079920-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079920A>G , CM000670.2:g.127079920A>G GRCh38
NC_000008.10:g.128092165A>G , CM000670.1:g.128092165A>G GRCh37
NC_000008.9:g.128161347A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.47A>G (PRNCR1)
NR_119373.1:n.102-787T>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'