Canonical Allele Identifier: CA15267668

Gene: CD96

Linked Data

• dbSNP Id: rs1489032
• gnomAD v2: 3-111052611-T-C
• gnomAD v3: 3-111333764-T-C
• gnomAD v4: 3-111333764-T-C
• MyVariant Identifiers: chr3:g.111052611T>C (hg19) ; chr3:g.111333764T>C (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333764T>C , CM000665.2:g.111333764T>C	GRCh38
NC_000003.11:g.111052611T>C , CM000665.1:g.111052611T>C	GRCh37
NC_000003.10:g.112535301T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000460744.1:c.-325-30749T>C	ENSP00000475194.1:n.-325-30749T>C
XR_924332.1:n.163+27246T>C