ClinGen Allele Registry
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Canonical Allele Identifier:
CA1818178472
Gene: PRNCR1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127091734T= , CM000670.2:g.127091734T=
GRCh38
NC_000008.10:g.128103979T= , CM000670.1:g.128103979T=
GRCh37
NC_000008.9:g.128173161T=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_109833.1:n.11861T=
Search 100 bp 5'
Search 100 bp 3'