Canonical Allele Identifier: CA81473777

Gene: CD96

Linked Data

• dbSNP Id: rs141847918
• gnomAD v2: 3-111052771-C-CA
• gnomAD v3: 3-111333924-C-CA
• gnomAD v4: 3-111333924-C-CA
• MyVariant Identifiers: chr3:g.111052771_111052772insA (hg19) ; chr3:g.111333924_111333925insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333932dup , CM000665.2:g.111333932dup	GRCh38
NC_000003.11:g.111052779dup , CM000665.1:g.111052779dup	GRCh37
NC_000003.10:g.112535469dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-30581dup	ENSP00000475194.1:n.-325-30581dup
XR_924332.1:n.163+27414dup