Canonical Allele Identifier: CA81473741
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs558378628
gnomAD v3: 3-111333685-C-T
gnomAD v4: 3-111333685-C-T
MyVariant Identifiers: chr3:g.111052532C>T (hg19) chr3:g.111333685C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333685C>T , CM000665.2:g.111333685C>T GRCh38
NC_000003.11:g.111052532C>T , CM000665.1:g.111052532C>T GRCh37
NC_000003.10:g.112535222C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000460744.1:c.-325-30828C>T ENSP00000475194.1:n.-325-30828C>T
XR_924332.1:n.163+27167C>T
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