Canonical Allele Identifier: CA586000481
Gene: CD274 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.5455732T>A
GRCh37 chr9:g.5455732T>A
gnomAD v2:
9:5455732 T / A
gnomAD v3:
9:5455732 T / A
gnomAD v4:
chr9-5455732-T-A
Joint Max Group AF 0.00001973 (NFE)
Genomes Max Group AF 0.00001973 (NFE)
dbSNP:
2282055
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455732T>A , CM000671.2:g.5455732T>A GRCh38
NC_000009.11:g.5455732T>A , CM000671.1:g.5455732T>A GRCh37
NC_000009.10:g.5445732T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381577.4:c.-14-368T>A MANE Select ENSP00000370989.3:n.-14-368T>A
ENST00000381573.8:c.-14-368T>A ENSP00000370985.4:n.-14-368T>A
ENST00000381577.3:c.-14-368T>A ENSP00000370989.3:n.-14-368T>A
NM_001267706.1:c.-14-368T>A NP_001254635.1:n.-14-368T>A
NM_001314029.1:c.-14-368T>A NP_001300958.1:n.-14-368T>A
NM_014143.3:c.-14-368T>A NP_054862.1:n.-14-368T>A
NR_052005.1:n.95-368T>A
XM_006716759.2:c.-14-368T>A XP_006716822.1:n.-14-368T>A
NM_014143.4:c.-14-368T>A MANE Select NP_054862.1:n.-14-368T>A
NM_001314029.2:c.-14-368T>A NP_001300958.1:n.-14-368T>A
NR_052005.2:n.56-368T>A
NM_001267706.2:c.-14-368T>A NP_001254635.1:n.-14-368T>A
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