Canonical Allele Identifier: CA897108481
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1218101606
gnomAD v3: 3-111333731-G-A
gnomAD v4: 3-111333731-G-A
MyVariant Identifiers: chr3:g.111052578G>A (hg19) chr3:g.111333731G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333731G>A , CM000665.2:g.111333731G>A GRCh38
NC_000003.11:g.111052578G>A , CM000665.1:g.111052578G>A GRCh37
NC_000003.10:g.112535268G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000460744.1:c.-325-30782G>A ENSP00000475194.1:n.-325-30782G>A
XR_924332.1:n.163+27213G>A
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