Canonical Allele Identifier: CA185699122
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs13252298
gnomAD v2: 8-128095156-A-G
gnomAD v3: 8-127082911-A-G
gnomAD v4: 8-127082911-A-G
MyVariant Identifiers: chr8:g.128095156A>G (hg19) chr8:g.127082911A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127082911A>G , CM000670.2:g.127082911A>G GRCh38
NC_000008.10:g.128095156A>G , CM000670.1:g.128095156A>G GRCh37
NC_000008.9:g.128164338A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.3038A>G
Search 100 bp 5'
Search 100 bp 3'