Canonical Allele Identifier: CA1393367779
Gene: CD96 HGNC NCBI

Linked Data

dbSNP Id: rs2037068642

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111333939A>G , CM000665.2:g.111333939A>G GRCh38
NC_000003.11:g.111052786A>G , CM000665.1:g.111052786A>G GRCh37
NC_000003.10:g.112535476A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000460744.1:c.-325-30574A>G ENSP00000475194.1:n.-325-30574A>G
XR_924332.1:n.163+27421A>G