Canonical Allele Identifier: CA185700249
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1036998669
MyVariant Identifiers: chr8:g.128104031C>G (hg19) chr8:g.127091786C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091786C>G , CM000670.2:g.127091786C>G GRCh38
NC_000008.10:g.128104031C>G , CM000670.1:g.128104031C>G GRCh37
NC_000008.9:g.128173213C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11913C>G
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Search 100 bp 3'