Canonical Allele Identifier: CA81473770

Gene: CD96

Linked Data

• dbSNP Id: rs1057054494
• gnomAD v2: 3-111052723-T-C
• gnomAD v3: 3-111333876-T-C
• gnomAD v4: 3-111333876-T-C
• MyVariant Identifiers: chr3:g.111052723T>C (hg19) ; chr3:g.111333876T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333876T>C , CM000665.2:g.111333876T>C	GRCh38
NC_000003.11:g.111052723T>C , CM000665.1:g.111052723T>C	GRCh37
NC_000003.10:g.112535413T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-30637T>C	ENSP00000475194.1:n.-325-30637T>C
XR_924332.1:n.163+27358T>C