Canonical Allele Identifier: CA897108378

Gene: CD96

Linked Data

• dbSNP Id: rs1231145586
• gnomAD v3: 3-111333426-G-C
• gnomAD v4: 3-111333426-G-C
• MyVariant Identifiers: chr3:g.111052273G>C (hg19) ; chr3:g.111333426G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333426G>C , CM000665.2:g.111333426G>C	GRCh38
NC_000003.11:g.111052273G>C , CM000665.1:g.111052273G>C	GRCh37
NC_000003.10:g.112534963G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-31087G>C	ENSP00000475194.1:n.-325-31087G>C
XR_924332.1:n.163+26908G>C