Canonical Allele Identifier: CA188503745
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs926855565
gnomAD v3: 9-5455648-G-A
gnomAD v4: 9-5455648-G-A
MyVariant Identifiers: chr9:g.5455648G>A (hg19) chr9:g.5455648G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455648G>A , CM000671.2:g.5455648G>A GRCh38
NC_000009.11:g.5455648G>A , CM000671.1:g.5455648G>A GRCh37
NC_000009.10:g.5445648G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.-14-452G>A MANE Select ENSP00000370989.3:n.-14-452G>A
ENST00000381573.8:c.-14-452G>A ENSP00000370985.4:n.-14-452G>A
ENST00000381577.3:c.-14-452G>A ENSP00000370989.3:n.-14-452G>A
NM_001267706.1:c.-14-452G>A NP_001254635.1:n.-14-452G>A
NM_001314029.1:c.-14-452G>A NP_001300958.1:n.-14-452G>A
NM_014143.3:c.-14-452G>A NP_054862.1:n.-14-452G>A
NR_052005.1:n.95-452G>A
XM_006716759.2:c.-14-452G>A XP_006716822.1:n.-14-452G>A
NM_014143.4:c.-14-452G>A MANE Select NP_054862.1:n.-14-452G>A
NM_001314029.2:c.-14-452G>A NP_001300958.1:n.-14-452G>A
NR_052005.2:n.56-452G>A
NM_001267706.2:c.-14-452G>A NP_001254635.1:n.-14-452G>A
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