Canonical Allele Identifier: CA81473708
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs141235563
gnomAD v3: 3-111333349-G-A
gnomAD v4: 3-111333349-G-A
MyVariant Identifiers: chr3:g.111052196G>A (hg19) chr3:g.111333349G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333349G>A , CM000665.2:g.111333349G>A GRCh38
NC_000003.11:g.111052196G>A , CM000665.1:g.111052196G>A GRCh37
NC_000003.10:g.112534886G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31164G>A ENSP00000475194.1:n.-325-31164G>A
XR_924332.1:n.163+26831G>A
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