Canonical Allele Identifier: CA897108347
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1171652120
gnomAD v3: 3-111333402-T-A
gnomAD v4: 3-111333402-T-A
MyVariant Identifiers: chr3:g.111052249T>A (hg19) chr3:g.111333402T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333402T>A , CM000665.2:g.111333402T>A GRCh38
NC_000003.11:g.111052249T>A , CM000665.1:g.111052249T>A GRCh37
NC_000003.10:g.112534939T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31111T>A ENSP00000475194.1:n.-325-31111T>A
XR_924332.1:n.163+26884T>A
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