Canonical Allele Identifier: CA585058088
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1181235641
gnomAD v2: 8-128103876-GTAATT-G
gnomAD v3: 8-127091631-GTAATT-G
gnomAD v4: 8-127091631-GTAATT-G
MyVariant Identifiers: chr8:g.128103877_128103881del (hg19) chr8:g.127091632_127091636del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091638_127091642del , CM000670.2:g.127091638_127091642del GRCh38
NC_000008.10:g.128103883_128103887del , CM000670.1:g.128103883_128103887del GRCh37
NC_000008.9:g.128173065_128173069del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11765_11769del
Search 100 bp 5'
Search 100 bp 3'