Canonical Allele Identifier: CA1118986255
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

gnomAD v3: 8-127080153-A-AAATAGTCTTTCAGGCCCTTTCCT
gnomAD v4: 8-127080153-A-AAATAGTCTTTCAGGCCCTTTCCT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080153_127080154insAATAGTCTTTCAGGCCCTTTCCT , CM000670.2:g.127080153_127080154insAATAGTCTTTCAGGCCCTTTCCT GRCh38
NC_000008.10:g.128092398_128092399insAATAGTCTTTCAGGCCCTTTCCT , CM000670.1:g.128092398_128092399insAATAGTCTTTCAGGCCCTTTCCT GRCh37
NC_000008.9:g.128161580_128161581insAATAGTCTTTCAGGCCCTTTCCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.280_281insAATAGTCTTTCAGGCCCTTTCCT (PRNCR1)
NR_119373.1:n.102-1021_102-1020insAGGAAAGGGCCTGAAAGACTATT (PCAT2)
Search 100 bp 5'
Search 100 bp 3'