Canonical Allele Identifier: CA847146659
Gene: PRNCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1209989206
MyVariant Identifiers: chr8:g.128103935_128103943del (hg19) chr8:g.127091690_127091698del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127091694_127091702del , CM000670.2:g.127091694_127091702del GRCh38
NC_000008.10:g.128103939_128103947del , CM000670.1:g.128103939_128103947del GRCh37
NC_000008.9:g.128173121_128173129del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.11821_11829del
Search 100 bp 5'
Search 100 bp 3'