Canonical Allele Identifier: CA2591488947
Gene: CD69 HGNC NCBI

Linked Data

dbSNP Id: rs2121101173
gnomAD v3: 12-9757447-C-A
gnomAD v4: 12-9757447-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757447C>A , CM000674.2:g.9757447C>A GRCh38
NC_000012.11:g.9910043C>A , CM000674.1:g.9910043C>A GRCh37
NC_000012.10:g.9801310C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228434.7:c.65-1028G>T MANE Select ENSP00000228434.3:n.65-1028G>T
ENST00000416624.6:n.146-1028G>T
ENST00000536709.1:c.65-1028G>T ENSP00000442597.1:n.65-1028G>T
ENST00000543147.1:n.146-1028G>T
NM_001781.2:c.65-1028G>T MANE Select NP_001772.1:n.65-1028G>T
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