Canonical Allele Identifier: CA185698804
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs532688845
gnomAD v2: 8-128092539-A-C
gnomAD v3: 8-127080294-A-C
gnomAD v4: 8-127080294-A-C
MyVariant Identifiers: chr8:g.128092539A>C (hg19) chr8:g.127080294A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080294A>C , CM000670.2:g.127080294A>C GRCh38
NC_000008.10:g.128092539A>C , CM000670.1:g.128092539A>C GRCh37
NC_000008.9:g.128161721A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.421A>C (PRNCR1)
NR_119373.1:n.102-1161T>G (PCAT2)
Search 100 bp 5'
Search 100 bp 3'