Canonical Allele Identifier: CA1393367629
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1450966230
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333638A>T , CM000665.2:g.111333638A>T GRCh38
NC_000003.11:g.111052485A>T , CM000665.1:g.111052485A>T GRCh37
NC_000003.10:g.112535175A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30875A>T ENSP00000475194.1:n.-325-30875A>T
XR_924332.1:n.163+27120A>T
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