Canonical Allele Identifier: CA232744488
Gene: CD69 HGNC NCBI

Linked Data

dbSNP Id: rs960367008
gnomAD v2: 12-9910163-C-T
gnomAD v3: 12-9757567-C-T
gnomAD v4: 12-9757567-C-T
MyVariant Identifiers: chr12:g.9910163C>T (hg19) chr12:g.9757567C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9757567C>T , CM000674.2:g.9757567C>T GRCh38
NC_000012.11:g.9910163C>T , CM000674.1:g.9910163C>T GRCh37
NC_000012.10:g.9801430C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000228434.7:c.65-1148G>A MANE Select ENSP00000228434.3:n.65-1148G>A
ENST00000416624.6:n.146-1148G>A
ENST00000536709.1:c.65-1148G>A ENSP00000442597.1:n.65-1148G>A
ENST00000543147.1:n.146-1148G>A
NM_001781.2:c.65-1148G>A MANE Select NP_001772.1:n.65-1148G>A
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