Canonical Allele Identifier: CA897108475
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs1184444081
gnomAD v3: 3-111333717-T-C
gnomAD v4: 3-111333717-T-C
MyVariant Identifiers: chr3:g.111052564T>C (hg19) chr3:g.111333717T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333717T>C , CM000665.2:g.111333717T>C GRCh38
NC_000003.11:g.111052564T>C , CM000665.1:g.111052564T>C GRCh37
NC_000003.10:g.112535254T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30796T>C ENSP00000475194.1:n.-325-30796T>C
XR_924332.1:n.163+27199T>C
Search 100 bp 5'
Search 100 bp 3'