Canonical Allele Identifier: CA81473714
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs34447624
gnomAD v2: 3-111052245-TG-T
gnomAD v3: 3-111333398-TG-T
gnomAD v4: 3-111333398-TG-T
MyVariant Identifiers: chr3:g.111052246del (hg19) chr3:g.111333399del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333400del , CM000665.2:g.111333400del GRCh38
NC_000003.11:g.111052247del , CM000665.1:g.111052247del GRCh37
NC_000003.10:g.112534937del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31113del ENSP00000475194.1:n.-325-31113del
XR_924332.1:n.163+26882del
Search 100 bp 5'
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