Canonical Allele Identifier: CA81473719

Gene: CD96

Linked Data

• dbSNP Id: rs972964852
• gnomAD v2: 3-111052288-A-G
• gnomAD v3: 3-111333441-A-G
• gnomAD v4: 3-111333441-A-G
• MyVariant Identifiers: chr3:g.111052288A>G (hg19) ; chr3:g.111333441A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333441A>G , CM000665.2:g.111333441A>G	GRCh38
NC_000003.11:g.111052288A>G , CM000665.1:g.111052288A>G	GRCh37
NC_000003.10:g.112534978A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-31072A>G	ENSP00000475194.1:n.-325-31072A>G
XR_924332.1:n.163+26923A>G