Canonical Allele Identifier: CA545480474
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1470540438
gnomAD v2: 3-111052740-T-G
gnomAD v3: 3-111333893-T-G
gnomAD v4: 3-111333893-T-G
MyVariant Identifiers: chr3:g.111052740T>G (hg19) chr3:g.111333893T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333893T>G , CM000665.2:g.111333893T>G GRCh38
NC_000003.11:g.111052740T>G , CM000665.1:g.111052740T>G GRCh37
NC_000003.10:g.112535430T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30620T>G ENSP00000475194.1:n.-325-30620T>G
XR_924332.1:n.163+27375T>G
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