Canonical Allele Identifier: CA10575848

Gene: CRIPT

Linked Data

• ClinVar Variation Id: 221619
• ClinVar RCV Id: RCV000240818
• MyVariant Identifiers: chr2:g.46844000_46845330del (hg19) ; chr2:g.46616861_46618191del (hg38)
• PubMed: PMID:27250922

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46616861_46618191del , CM000664.2:g.46616861_46618191del	GRCh38
NC_000002.11:g.46844000_46845330del , CM000664.1:g.46844000_46845330del	GRCh37
NC_000002.10:g.46697504_46698834del	NCBI36
NG_034144.1:g.4690_6020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486447.1:n.446_609-582del