Canonical Allele Identifier: CA2688533592
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

gnomAD v4: 8-127081066-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081066A>G , CM000670.2:g.127081066A>G GRCh38
NC_000008.10:g.128093311A>G , CM000670.1:g.128093311A>G GRCh37
NC_000008.9:g.128162493A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.1193A>G (PRNCR1)
NR_119373.1:n.101+1055T>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'