Canonical Allele Identifier: CA603247962
Gene: CD69 HGNC NCBI

Linked Data

dbSNP Id: rs1395272241
gnomAD v2: 12-9910046-T-C
gnomAD v3: 12-9757450-T-C
gnomAD v4: 12-9757450-T-C
MyVariant Identifiers: chr12:g.9910046T>C (hg19) chr12:g.9757450T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757450T>C , CM000674.2:g.9757450T>C GRCh38
NC_000012.11:g.9910046T>C , CM000674.1:g.9910046T>C GRCh37
NC_000012.10:g.9801313T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000228434.7:c.65-1031A>G MANE Select ENSP00000228434.3:n.65-1031A>G
ENST00000416624.6:n.146-1031A>G
ENST00000536709.1:c.65-1031A>G ENSP00000442597.1:n.65-1031A>G
ENST00000543147.1:n.146-1031A>G
NM_001781.2:c.65-1031A>G MANE Select NP_001772.1:n.65-1031A>G
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