Canonical Allele Identifier: CA81473796
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs994253220
gnomAD v2: 3-111052917-T-G
gnomAD v3: 3-111334070-T-G
gnomAD v4: 3-111334070-T-G
MyVariant Identifiers: chr3:g.111052917T>G (hg19) chr3:g.111334070T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111334070T>G , CM000665.2:g.111334070T>G GRCh38
NC_000003.11:g.111052917T>G , CM000665.1:g.111052917T>G GRCh37
NC_000003.10:g.112535607T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30443T>G ENSP00000475194.1:n.-325-30443T>G
XR_924332.1:n.163+27552T>G
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