Canonical Allele Identifier: CA185698774
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1000210070
gnomAD v3: 8-127079922-A-G
gnomAD v4: 8-127079922-A-G
MyVariant Identifiers: chr8:g.128092167A>G (hg19) chr8:g.127079922A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079922A>G , CM000670.2:g.127079922A>G GRCh38
NC_000008.10:g.128092167A>G , CM000670.1:g.128092167A>G GRCh37
NC_000008.9:g.128161349A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.49A>G (PRNCR1)
NR_119373.1:n.102-789T>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'