Canonical Allele Identifier: CA81473746
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs766496453
gnomAD v2: 3-111052561-A-G
gnomAD v3: 3-111333714-A-G
gnomAD v4: 3-111333714-A-G
MyVariant Identifiers: chr3:g.111052561A>G (hg19) chr3:g.111333714A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333714A>G , CM000665.2:g.111333714A>G GRCh38
NC_000003.11:g.111052561A>G , CM000665.1:g.111052561A>G GRCh37
NC_000003.10:g.112535251A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30799A>G ENSP00000475194.1:n.-325-30799A>G
XR_924332.1:n.163+27196A>G
Search 100 bp 5'
Search 100 bp 3'