Canonical Allele Identifier: CA897108626
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1205002413
gnomAD v3: 3-111334077-T-TA
gnomAD v4: 3-111334077-T-TA
MyVariant Identifiers: chr3:g.111052924_111052925insA (hg19) chr3:g.111334077_111334078insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111334078dup , CM000665.2:g.111334078dup GRCh38
NC_000003.11:g.111052925dup , CM000665.1:g.111052925dup GRCh37
NC_000003.10:g.112535615dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30435dup ENSP00000475194.1:n.-325-30435dup
XR_924332.1:n.163+27560dup
Search 100 bp 5'
Search 100 bp 3'