Canonical Allele Identifier: CA2688537976
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs2130317593
gnomAD v4: 8-127092079-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127092079A>C , CM000670.2:g.127092079A>C GRCh38
NC_000008.10:g.128104324A>C , CM000670.1:g.128104324A>C GRCh37
NC_000008.9:g.128173506A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.12206A>C
Search 100 bp 5'
Search 100 bp 3'