Canonical Allele Identifier: CA185698782
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs982946130
gnomAD v2: 8-128092321-C-T
gnomAD v3: 8-127080076-C-T
gnomAD v4: 8-127080076-C-T
MyVariant Identifiers: chr8:g.128092321C>T (hg19) chr8:g.127080076C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080076C>T , CM000670.2:g.127080076C>T GRCh38
NC_000008.10:g.128092321C>T , CM000670.1:g.128092321C>T GRCh37
NC_000008.9:g.128161503C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.203C>T (PRNCR1)
NR_119373.1:n.102-943G>A (PCAT2)
Search 100 bp 5'
Search 100 bp 3'