Canonical Allele Identifier: CA585055353
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1341176267
gnomAD v2: 8-128092542-A-G
gnomAD v3: 8-127080297-A-G
gnomAD v4: 8-127080297-A-G
MyVariant Identifiers: chr8:g.128092542A>G (hg19) chr8:g.127080297A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080297A>G , CM000670.2:g.127080297A>G GRCh38
NC_000008.10:g.128092542A>G , CM000670.1:g.128092542A>G GRCh37
NC_000008.9:g.128161724A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.424A>G (PRNCR1)
NR_119373.1:n.102-1164T>C (PCAT2)
Search 100 bp 5'
Search 100 bp 3'