Canonical Allele Identifier: CA897108360
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1479130804
MyVariant Identifiers: chr3:g.111052253_111052257del (hg19) chr3:g.111333406_111333410del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333407_111333411del , CM000665.2:g.111333407_111333411del GRCh38
NC_000003.11:g.111052254_111052258del , CM000665.1:g.111052254_111052258del GRCh37
NC_000003.10:g.112534944_112534948del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31106_-325-31102del ENSP00000475194.1:n.-325-31106_-325-31102del
XR_924332.1:n.163+26889_163+26893del
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