Canonical Allele Identifier: CA545480478
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs531875819
gnomAD v2: 3-111052762-G-C
MyVariant Identifiers: chr3:g.111052762G>C (hg19) chr3:g.111333915G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333915G>C , CM000665.2:g.111333915G>C GRCh38
NC_000003.11:g.111052762G>C , CM000665.1:g.111052762G>C GRCh37
NC_000003.10:g.112535452G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30598G>C ENSP00000475194.1:n.-325-30598G>C
XR_924332.1:n.163+27397G>C
Search 100 bp 5'
Search 100 bp 3'