Canonical Allele Identifier: CA897108310
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1216159915
gnomAD v3: 3-111333332-G-C
gnomAD v4: 3-111333332-G-C
MyVariant Identifiers: chr3:g.111052179G>C (hg19) chr3:g.111333332G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333332G>C , CM000665.2:g.111333332G>C GRCh38
NC_000003.11:g.111052179G>C , CM000665.1:g.111052179G>C GRCh37
NC_000003.10:g.112534869G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31181G>C ENSP00000475194.1:n.-325-31181G>C
XR_924332.1:n.163+26814G>C
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