Canonical Allele Identifier: CA1118986176
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813580149
gnomAD v3: 8-127079985-C-A
gnomAD v4: 8-127079985-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079985C>A , CM000670.2:g.127079985C>A GRCh38
NC_000008.10:g.128092230C>A , CM000670.1:g.128092230C>A GRCh37
NC_000008.9:g.128161412C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.112C>A (PRNCR1)
NR_119373.1:n.102-852G>T (PCAT2)
Search 100 bp 5'
Search 100 bp 3'