Canonical Allele Identifier: CA944641176

Gene: CD69

Linked Data

• dbSNP Id: rs1866688581
• gnomAD v3: 12-9757440-C-CAA
• gnomAD v4: 12-9757440-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9757443_9757444dup , CM000674.2:g.9757443_9757444dup	GRCh38
NC_000012.11:g.9910039_9910040dup , CM000674.1:g.9910039_9910040dup	GRCh37
NC_000012.10:g.9801306_9801307dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000228434.7:c.65-1023_65-1022dup MANE Select	ENSP00000228434.3:n.65-1023_65-1022dup
ENST00000416624.6:n.146-1023_146-1022dup
ENST00000536709.1:c.65-1023_65-1022dup	ENSP00000442597.1:n.65-1023_65-1022dup
ENST00000543147.1:n.146-1023_146-1022dup
NM_001781.2:c.65-1023_65-1022dup MANE Select	NP_001772.1:n.65-1023_65-1022dup