Canonical Allele Identifier: CA435182000
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs2037068736
gnomAD v3: 3-111333958-C-A
gnomAD v4: 3-111333958-C-A
MyVariant Identifiers: chr3:g.111052805C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333958C>A , CM000665.2:g.111333958C>A GRCh38
NC_000003.11:g.111052805C>A , CM000665.1:g.111052805C>A GRCh37
NC_000003.10:g.112535495C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30555C>A ENSP00000475194.1:n.-325-30555C>A
XR_924332.1:n.163+27440C>A
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