Canonical Allele Identifier: CA188513325
Gene: CD274 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.5470497A>G
GRCh37 chr9:g.5470497A>G
gnomAD v2:
9:5470497 A / G
gnomAD v3:
9:5470497 A / G
gnomAD v4:
chr9-5470497-A-G
Joint Max Group AF 0.51086509 (EAS)
Genomes Max Group AF 0.51893791 (EAS)
Exomes Max Group AF 0.50010853 (EAS)
ClinVar RCV:
RCV001650442
ClinVar Variation:
1251890
dbSNP:
4742098
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5470497A>G , CM000671.2:g.5470497A>G GRCh38
NC_000009.11:g.5470497A>G , CM000671.1:g.5470497A>G GRCh37
NC_000009.10:g.5460497A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381577.4:c.*2635A>G MANE Select ENSP00000370989.3:n.*2635A>G
ENST00000381573.8:c.*2635A>G ENSP00000370985.4:n.*2635A>G
ENST00000381577.3:c.*2635A>G ENSP00000370989.3:n.*2635A>G
NM_001267706.1:c.*2635A>G NP_001254635.1:n.*2635A>G
NM_014143.3:c.*2635A>G NP_054862.1:n.*2635A>G
NR_052005.1:n.3443A>G
NM_014143.4:c.*2635A>G MANE Select NP_054862.1:n.*2635A>G
NR_052005.2:n.3404A>G
NM_001267706.2:c.*2635A>G NP_001254635.1:n.*2635A>G
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