Canonical Allele Identifier: CA585055303
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1405900569
gnomAD v2: 8-128092118-T-TA
gnomAD v3: 8-127079873-T-TA
gnomAD v4: 8-127079873-T-TA
MyVariant Identifiers: chr8:g.128092118_128092119insA (hg19) chr8:g.127079873_127079874insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079876dup , CM000670.2:g.127079876dup GRCh38
NC_000008.10:g.128092121dup , CM000670.1:g.128092121dup GRCh37
NC_000008.9:g.128161303dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.3dup (PRNCR1)
NR_119373.1:n.102-741dup (PCAT2)
Search 100 bp 5'
Search 100 bp 3'