Canonical Allele Identifier: CA2015631600
Gene: CD69 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757459A= , CM000674.2:g.9757459A= GRCh38
NC_000012.11:g.9910055A= , CM000674.1:g.9910055A= GRCh37
NC_000012.10:g.9801322A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228434.7:c.65-1040T= MANE Select ENSP00000228434.3:n.65-1040T=
ENST00000416624.6:n.146-1040T=
ENST00000536709.1:c.65-1040T= ENSP00000442597.1:n.65-1040T=
ENST00000543147.1:n.146-1040T=
NM_001781.2:c.65-1040T= MANE Select NP_001772.1:n.65-1040T=
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