Canonical Allele Identifier: CA185698781
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs953027373
gnomAD v2: 8-128092304-A-G
gnomAD v3: 8-127080059-A-G
gnomAD v4: 8-127080059-A-G
MyVariant Identifiers: chr8:g.128092304A>G (hg19) chr8:g.127080059A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080059A>G , CM000670.2:g.127080059A>G GRCh38
NC_000008.10:g.128092304A>G , CM000670.1:g.128092304A>G GRCh37
NC_000008.9:g.128161486A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.186A>G (PRNCR1)
NR_119373.1:n.102-926T>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'