Canonical Allele Identifier: CA81473780
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs149202090
gnomAD v2: 3-111052778-A-T
gnomAD v3: 3-111333931-A-T
gnomAD v4: 3-111333931-A-T
MyVariant Identifiers: chr3:g.111052778A>T (hg19) chr3:g.111333931A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333931A>T , CM000665.2:g.111333931A>T GRCh38
NC_000003.11:g.111052778A>T , CM000665.1:g.111052778A>T GRCh37
NC_000003.10:g.112535468A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30582A>T ENSP00000475194.1:n.-325-30582A>T
XR_924332.1:n.163+27413A>T
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