Canonical Allele Identifier: CA847139011
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1222636523
MyVariant Identifiers: chr8:g.128092540_128092541insA (hg19) chr8:g.127080295_127080296insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080297dup , CM000670.2:g.127080297dup GRCh38
NC_000008.10:g.128092542dup , CM000670.1:g.128092542dup GRCh37
NC_000008.9:g.128161724dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.424dup (PRNCR1)
NR_119373.1:n.102-1163dup (PCAT2)
Search 100 bp 5'
Search 100 bp 3'