Canonical Allele Identifier: CA81473755

Gene: CD96

Linked Data

• dbSNP Id: rs934457979
• MyVariant Identifiers: chr3:g.111052637C>T (hg19) ; chr3:g.111333790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111333790C>T , CM000665.2:g.111333790C>T	GRCh38
NC_000003.11:g.111052637C>T , CM000665.1:g.111052637C>T	GRCh37
NC_000003.10:g.112535327C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-30723C>T	ENSP00000475194.1:n.-325-30723C>T
XR_924332.1:n.163+27272C>T