Canonical Allele Identifier: CA1393367761
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs2037068401

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333921A>C , CM000665.2:g.111333921A>C GRCh38
NC_000003.11:g.111052768A>C , CM000665.1:g.111052768A>C GRCh37
NC_000003.10:g.112535458A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30592A>C ENSP00000475194.1:n.-325-30592A>C
XR_924332.1:n.163+27403A>C