Canonical Allele Identifier: CA2604535398
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2130303198
gnomAD v3: 8-127081061-C-G
gnomAD v4: 8-127081061-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127081061C>G , CM000670.2:g.127081061C>G GRCh38
NC_000008.10:g.128093306C>G , CM000670.1:g.128093306C>G GRCh37
NC_000008.9:g.128162488C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.1188C>G (PRNCR1)
NR_119373.1:n.101+1060G>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'