Canonical Allele Identifier: CA847146773

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1243929624
• gnomAD v3: 8-127091854-AACTTCT-A
• gnomAD v4: 8-127091854-AACTTCT-A
• MyVariant Identifiers: chr8:g.128104100_128104105del (hg19) ; chr8:g.127091855_127091860del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091860_127091865del , CM000670.2:g.127091860_127091865del	GRCh38
NC_000008.10:g.128104105_128104110del , CM000670.1:g.128104105_128104110del	GRCh37
NC_000008.9:g.128173287_128173292del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11987_11992del