Canonical Allele Identifier: CA897108583
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1280781039
gnomAD v3: 3-111333971-TTAAA-T
gnomAD v4: 3-111333971-TTAAA-T
MyVariant Identifiers: chr3:g.111052819_111052822del (hg19) chr3:g.111333972_111333975del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333978_111333981del , CM000665.2:g.111333978_111333981del GRCh38
NC_000003.11:g.111052825_111052828del , CM000665.1:g.111052825_111052828del GRCh37
NC_000003.10:g.112535515_112535518del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30535_-325-30532del ENSP00000475194.1:n.-325-30535_-325-30532del
XR_924332.1:n.163+27460_163+27463del
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