Canonical Allele Identifier: CA847146738

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1412425053
• gnomAD v3: 8-127091810-GGGATTATTTGGA-G
• gnomAD v4: 8-127091810-GGGATTATTTGGA-G
• MyVariant Identifiers: chr8:g.128104056_128104067del (hg19) ; chr8:g.127091811_127091822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091811_127091822del , CM000670.2:g.127091811_127091822del	GRCh38
NC_000008.10:g.128104056_128104067del , CM000670.1:g.128104056_128104067del	GRCh37
NC_000008.9:g.128173238_128173249del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11938_11949del