Canonical Allele Identifier: CA897108400
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1444740928
gnomAD v3: 3-111333493-AT-A
gnomAD v4: 3-111333493-AT-A
MyVariant Identifiers: chr3:g.111052341del (hg19) chr3:g.111333494del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333498del , CM000665.2:g.111333498del GRCh38
NC_000003.11:g.111052345del , CM000665.1:g.111052345del GRCh37
NC_000003.10:g.112535035del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31015del ENSP00000475194.1:n.-325-31015del
XR_924332.1:n.163+26980del
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