Canonical Allele Identifier: CA81473723
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs527629904
gnomAD v3: 3-111333465-G-A
gnomAD v4: 3-111333465-G-A
MyVariant Identifiers: chr3:g.111052312G>A (hg19) chr3:g.111333465G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333465G>A , CM000665.2:g.111333465G>A GRCh38
NC_000003.11:g.111052312G>A , CM000665.1:g.111052312G>A GRCh37
NC_000003.10:g.112535002G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-31048G>A ENSP00000475194.1:n.-325-31048G>A
XR_924332.1:n.163+26947G>A
Search 100 bp 5'
Search 100 bp 3'