Canonical Allele Identifier: CA585058101

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1468244911
• gnomAD v2: 8-128103967-AAC-A
• gnomAD v3: 8-127091722-AAC-A
• gnomAD v4: 8-127091722-AAC-A
• MyVariant Identifiers: chr8:g.128103968_128103969del (hg19) ; chr8:g.127091723_127091724del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091724_127091725del , CM000670.2:g.127091724_127091725del	GRCh38
NC_000008.10:g.128103969_128103970del , CM000670.1:g.128103969_128103970del	GRCh37
NC_000008.9:g.128173151_128173152del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11851_11852del