Canonical Allele Identifier: CA185700236

Gene: PRNCR1

Linked Data

• dbSNP Id: rs765449645
• MyVariant Identifiers: chr8:g.128103969_128103973del (hg19) ; chr8:g.127091724_127091728del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091724_127091728del , CM000670.2:g.127091724_127091728del	GRCh38
NC_000008.10:g.128103969_128103973del , CM000670.1:g.128103969_128103973del	GRCh37
NC_000008.9:g.128173151_128173155del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11851_11855del