Canonical Allele Identifier: CA1118986195
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813581012
gnomAD v3: 8-127080047-T-C
gnomAD v4: 8-127080047-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080047T>C , CM000670.2:g.127080047T>C GRCh38
NC_000008.10:g.128092292T>C , CM000670.1:g.128092292T>C GRCh37
NC_000008.9:g.128161474T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.174T>C (PRNCR1)
NR_119373.1:n.102-914A>G (PCAT2)
Search 100 bp 5'
Search 100 bp 3'