Canonical Allele Identifier: CA1052222408
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs2037069440
gnomAD v3: 3-111334077-T-C
gnomAD v4: 3-111334077-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111334077T>C , CM000665.2:g.111334077T>C GRCh38
NC_000003.11:g.111052924T>C , CM000665.1:g.111052924T>C GRCh37
NC_000003.10:g.112535614T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30436T>C ENSP00000475194.1:n.-325-30436T>C
XR_924332.1:n.163+27559T>C
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