Canonical Allele Identifier: CA15121141
Gene: CD84 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.160546518A>G
GRCh37 chr1:g.160516308A>G
gnomAD v2:
1:160516308 A / G
gnomAD v3:
1:160546518 A / G
gnomAD v4:
chr1-160546518-A-G
Joint Max Group AF 0.90306526 (NFE)
Genomes Max Group AF 0.90306956 (NFE)
Exomes Max Group AF 0.72682072 (NFE)
dbSNP:
6427528
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160546518A>G , CM000663.2:g.160546518A>G GRCh38
NC_000001.10:g.160516308A>G , CM000663.1:g.160516308A>G GRCh37
NC_000001.9:g.158782932A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368054.8:c.*1738T>C MANE Select ENSP00000357033.4:n.*1738T>C
ENST00000368054.7:c.*1738T>C ENSP00000357033.3:n.*1738T>C
ENST00000534968.5:c.*1738T>C ENSP00000442845.1:n.*1738T>C
NM_001184879.1:c.*1738T>C NP_001171808.1:n.*1738T>C
NM_001184881.1:c.*1808T>C NP_001171810.1:n.*1808T>C
NM_001184882.1:c.*1738T>C NP_001171811.1:n.*1738T>C
NM_003874.3:c.*1738T>C NP_003865.1:n.*1738T>C
XM_011510094.1:c.*1738T>C XP_011508396.1:n.*1738T>C
XM_011510095.1:c.*1738T>C XP_011508397.1:n.*1738T>C
XR_922203.1:n.611+9331A>G
NM_001330742.1:c.*1738T>C NP_001317671.1:n.*1738T>C
XM_011510095.2:c.*1738T>C XP_011508397.1:n.*1738T>C
XR_002957960.1:n.5453T>C
XR_922203.2:n.1541+9331A>G
NM_001184879.2:c.*1738T>C NP_001171808.1:n.*1738T>C
NM_001184881.2:c.*1808T>C NP_001171810.1:n.*1808T>C
NM_001330742.2:c.*1738T>C NP_001317671.1:n.*1738T>C
NM_003874.4:c.*1738T>C MANE Select NP_003865.1:n.*1738T>C
NM_001184882.2:c.*1738T>C NP_001171811.1:n.*1738T>C
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