Canonical Allele Identifier: CA81473779

Gene: CD96

Linked Data

• dbSNP Id: rs544871495
• gnomAD v2: 3-111052773-A-C
• gnomAD v3: 3-111333926-A-C
• gnomAD v4: 3-111333926-A-C
• MyVariant Identifiers: chr3:g.111052773A>C (hg19) ; chr3:g.111333926A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333926A>C , CM000665.2:g.111333926A>C	GRCh38
NC_000003.11:g.111052773A>C , CM000665.1:g.111052773A>C	GRCh37
NC_000003.10:g.112535463A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-30587A>C	ENSP00000475194.1:n.-325-30587A>C
XR_924332.1:n.163+27408A>C