Canonical Allele Identifier: CA15757145
Gene: CD69 HGNC NCBI

Linked Data

dbSNP Id: rs4763879

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757568G>A , CM000674.2:g.9757568G>A GRCh38
NC_000012.11:g.9910164G>A , CM000674.1:g.9910164G>A GRCh37
NC_000012.10:g.9801431G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000228434.7:c.65-1149C>T ENSP00000228434.3:p.=
ENST00000536709.1:c.65-1149C>T ENSP00000442597.1:p.=
NM_001781.2:c.65-1149C>T MANE Select NP_001772.1:p.=