Canonical Allele Identifier: CA897108620

Gene: CD96

Linked Data

• dbSNP Id: rs994253220
• MyVariant Identifiers: chr3:g.111052917T>C (hg19) ; chr3:g.111334070T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111334070T>C , CM000665.2:g.111334070T>C	GRCh38
NC_000003.11:g.111052917T>C , CM000665.1:g.111052917T>C	GRCh37
NC_000003.10:g.112535607T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460744.1:c.-325-30443T>C	ENSP00000475194.1:n.-325-30443T>C
XR_924332.1:n.163+27552T>C